Unnati Pharmax

Mytera 250 mg Tablets
Composition: Abiraterone Acetate 250 mg
International Trade Name: Zytiga®

Mytera 250 mg Tablets are a high-quality formulation of Abiraterone Acetate, a selective androgen biosynthesis inhibitor, and a generic equivalent of the internationally recognized product marketed under the brand name Zytiga®. Manufactured in WHO-GMP certified facilities, Mytera Tablets are supplied by trusted pharmaceutical exporters from India to support advanced global oncology treatment programs, particularly in the management of prostate cancer.

Abiraterone acetate is a potent inhibitor of the CYP17 enzyme (17α-hydroxylase/C17,20-lyase), which plays a key role in androgen production. By suppressing androgen synthesis in the testes, adrenal glands, and tumor tissue, Mytera helps reduce testosterone levels and slows tumor growth and disease progression. This targeted hormonal therapy is typically administered in combination with prednisone or prednisolone.

Mytera 250 mg Tablets are primarily indicated for the treatment of metastatic castration-resistant prostate cancer (mCRPC) and metastatic hormone-sensitive prostate cancer (mHSPC), especially in patients who are receiving or have progressed on androgen deprivation therapy (ADT).

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Mytera Tablets are manufactured under stringent GMP and international pharmaceutical quality standards, ensuring consistent potency, safety, and long-term stability. The product is supplied in secure, tamper-proof, export-grade packaging with complete regulatory documentation, making it suitable for oncology clinics, tertiary care hospitals, government cancer programs, and international pharmaceutical distributors.

Abiranamo Tablets
Composition: Abiraterone Acetate Tablets (250 mg / 500 mg – as applicable)
International Trade Name: Zytiga®

Abiranamo is a high-quality Abiraterone Acetate formulation, a generic equivalent of the internationally recognized androgen biosynthesis inhibitor marketed under the brand name Zytiga®. Manufactured in WHO-GMP certified facilities, Abiranamo Tablets are supplied by trusted pharmaceutical exporters from India to support advanced global oncology treatment programs, particularly in prostate cancer therapy.

Abiraterone acetate is a selective and irreversible inhibitor of the CYP17 enzyme, which plays a crucial role in androgen production. By blocking androgen synthesis in the testes, adrenal glands, and tumor microenvironment, Abiranamo helps reduce circulating androgen levels, thereby slowing tumor growth and disease progression in hormone-dependent prostate cancer.

Abiranamo is primarily indicated for the treatment of metastatic castration-resistant prostate cancer (mCRPC) and metastatic hormone-sensitive prostate cancer (mHSPC). It is commonly administered in combination with prednisone or prednisolone as part of a comprehensive hormonal therapy regimen.

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Abiranamo Tablets are manufactured under stringent GMP and international pharmaceutical quality standards, ensuring consistent potency, safety, and long-term stability. The product is supplied in secure, tamper-proof, export-grade packaging with complete regulatory documentation, making it suitable for oncology clinics, tertiary care hospitals, government cancer programs, and international pharmaceutical distributors.

Indenza – Enzalutamide Capsules
Composition: Enzalutamide
International Trade Name: Xtandi®

Indenza is a high-quality formulation of Enzalutamide, a non-steroidal androgen receptor signaling inhibitor and a generic equivalent of the internationally recognized product marketed under the brand name Xtandi®. Manufactured in WHO-GMP certified facilities, Indenza is supplied by trusted pharmaceutical exporters from India to support advanced global oncology treatment programs, particularly in the management of advanced and metastatic prostate cancer.

Enzalutamide works by blocking multiple steps in the androgen receptor signaling pathway, including androgen binding, nuclear translocation, and DNA transcription. By effectively inhibiting these mechanisms, Indenza helps prevent prostate cancer cell proliferation and slows disease progression, even in patients resistant to conventional androgen deprivation therapy (ADT).

Indenza is primarily indicated for the treatment of metastatic castration-resistant prostate cancer (mCRPC), non-metastatic castration-resistant prostate cancer (nmCRPC), and metastatic hormone-sensitive prostate cancer (mHSPC). It can be prescribed as monotherapy or in combination with ongoing ADT.

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Indenza is manufactured under stringent GMP and international pharmaceutical quality standards, ensuring consistent efficacy, safety, and long-term stability. The product is supplied in secure, tamper-proof, export-grade packaging with complete regulatory documentation, making it suitable for oncology clinics, tertiary care hospitals, government cancer programs, and international pharmaceutical distributors.

Mytera 500 Tablets
Composition: Abiraterone Acetate 500 mg
International Trade Name: Zytiga®

Mytera 500 is a high-quality Abiraterone Acetate 500 mg tablet, a generic equivalent of the internationally recognized androgen biosynthesis inhibitor marketed under the brand name Zytiga®. Manufactured in WHO-GMP certified facilities, Mytera Tablets are supplied by trusted pharmaceutical exporters from India to support advanced global oncology treatment programs, particularly in the management of prostate cancer.

Abiraterone acetate is a potent, selective inhibitor of the CYP17 enzyme (17α-hydroxylase/C17,20-lyase), which is essential for androgen production. By suppressing androgen synthesis in the testes, adrenal glands, and tumor tissue, Mytera 500 helps reduce circulating testosterone levels, thereby slowing tumor growth and disease progression. This targeted hormonal therapy is typically administered in combination with prednisone or prednisolone.

Mytera 500 mg Tablets are primarily indicated for the treatment of metastatic castration-resistant prostate cancer (mCRPC) and metastatic hormone-sensitive prostate cancer (mHSPC), especially in patients who are receiving or have progressed on androgen deprivation therapy (ADT).

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Mytera Tablets are manufactured under stringent GMP and international pharmaceutical quality standards, ensuring consistent potency, safety, and long-term stability. The product is supplied in secure, tamper-proof, export-grade packaging with complete regulatory documentation, making it suitable for oncology clinics, tertiary care hospitals, government cancer programs, and international pharmaceutical distributors.

Abirapro 250 mg Tablets
Composition: Abiraterone Acetate 250 mg
International Trade Name: Zytiga®

Abirapro 250 mg Tablets are a high-quality formulation of Abiraterone Acetate, a selective androgen biosynthesis inhibitor, and a generic equivalent of the internationally recognized product marketed under the brand name Zytiga®. Manufactured in WHO-GMP certified facilities, Abirapro Tablets are supplied by trusted pharmaceutical exporters from India to support advanced global oncology treatment programs, particularly in the management of prostate cancer.

Abiraterone acetate is a potent inhibitor of the CYP17 enzyme (17α-hydroxylase/C17,20-lyase), which plays a key role in androgen production. By suppressing androgen synthesis in the testes, adrenal glands, and tumor tissue, Abirapro helps reduce testosterone levels and slows tumor growth and disease progression. This targeted hormonal therapy is typically administered in combination with prednisone or prednisolone.

Abirapro 250 mg Tablets are primarily indicated for the treatment of metastatic castration-resistant prostate cancer (mCRPC) and metastatic hormone-sensitive prostate cancer (mHSPC), especially in patients who are receiving or have progressed on androgen deprivation therapy (ADT).

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Abirapro Tablets are manufactured under stringent GMP and international pharmaceutical quality standards, ensuring consistent potency, safety, and long-term stability. The product is supplied in secure, tamper-proof, export-grade packaging with complete regulatory documentation, making it suitable for oncology clinics, tertiary care hospitals, government cancer programs, and international pharmaceutical distributors.

Samptica 500 Tablets
Composition: Abiraterone Acetate 500 mg
International Trade Name: Zytiga®, Yonsa®

Samptica 500 Tablets are a high-quality formulation of Abiraterone Acetate 500 mg, a selective androgen biosynthesis inhibitor, and a generic equivalent of the internationally recognized products marketed under the brand names Zytiga® and Yonsa®. Manufactured in WHO-GMP certified facilities, Samptica Tablets are supplied by trusted pharmaceutical exporters from India to support advanced global oncology treatment programs, particularly in the management of prostate cancer.

Abiraterone acetate works by selectively inhibiting the CYP17 enzyme (17α-hydroxylase/C17,20-lyase), which is critical for androgen production. By suppressing androgen synthesis in the testes, adrenal glands, and tumor tissue, Samptica 500 helps reduce circulating testosterone levels, thereby slowing tumor growth and disease progression. This targeted hormonal therapy is typically administered in combination with prednisone or prednisolone.

Samptica 500 mg Tablets are primarily indicated for the treatment of metastatic castration-resistant prostate cancer (mCRPC) and metastatic hormone-sensitive prostate cancer (mHSPC), especially in patients who are receiving or have progressed on androgen deprivation therapy (ADT).

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Samptica Tablets are manufactured under stringent GMP and international pharmaceutical quality standards, ensuring consistent potency, safety, and long-term stability. The product is supplied in secure, tamper-proof, export-grade packaging with complete regulatory documentation, making it suitable for oncology clinics, tertiary care hospitals, government cancer programs, and international pharmaceutical distributors.

Abirakast 250 mg Tablets
Composition: Abiraterone Acetate 250 mg Tablets
International Trade Name: Zytiga®

Abirakast 250 is a high-quality Abiraterone Acetate 250 mg tablet, a generic equivalent of the internationally recognized androgen biosynthesis inhibitor marketed under the brand name Zytiga®. Manufactured in WHO-GMP certified facilities, Abirakast Tablets are supplied by trusted pharmaceutical exporters from India to support advanced global oncology treatment programs, particularly in the management of prostate cancer.

Abiraterone acetate is a potent, selective inhibitor of the CYP17 enzyme (17α-hydroxylase/C17,20-lyase), which plays a key role in androgen biosynthesis. By suppressing androgen production in the testes, adrenal glands, and tumor tissues, Abirakast 250 helps reduce testosterone levels and slow disease progression. This targeted hormonal therapy is commonly administered in combination with prednisone or prednisolone.

Abirakast 250 mg Tablets are primarily indicated for the treatment of metastatic castration-resistant prostate cancer (mCRPC) and metastatic hormone-sensitive prostate cancer (mHSPC), particularly in patients undergoing or previously treated with androgen deprivation therapy (ADT).

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Abirakast Tablets are manufactured under stringent GMP and international pharmaceutical quality standards, ensuring consistent potency, safety, and long-term stability. The product is supplied in secure, tamper-proof, export-grade packaging with complete regulatory documentation, making it suitable for oncology clinics, tertiary care hospitals, government cancer programs, and international pharmaceutical distributors.

Bdron 250 Tablets
Composition: Abiraterone Acetate 250 mg
International Trade Name: Zytiga®

Bdron 250 Tablets are a high-quality formulation of Abiraterone Acetate 250 mg, a selective androgen biosynthesis inhibitor, and a generic equivalent of the internationally recognized product marketed under the brand name Zytiga®. Manufactured in WHO-GMP certified facilities, Bdron Tablets are supplied by trusted pharmaceutical exporters from India to support advanced global oncology treatment programs, particularly in the management of prostate cancer.

Abiraterone acetate works by selectively inhibiting the CYP17 enzyme (17α-hydroxylase/C17,20-lyase), which is essential for androgen production. By suppressing androgen synthesis in the testes, adrenal glands, and tumor tissue, Bdron 250 helps reduce circulating testosterone levels, thereby slowing tumor growth and disease progression. This targeted hormonal therapy is typically administered in combination with prednisone or prednisolone.

Bdron 250 mg Tablets are primarily indicated for the treatment of metastatic castration-resistant prostate cancer (mCRPC) and metastatic hormone-sensitive prostate cancer (mHSPC), especially in patients who are receiving or have progressed on androgen deprivation therapy (ADT).

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Bdron Tablets are manufactured under stringent GMP and international pharmaceutical quality standards, ensuring consistent potency, safety, and long-term stability. The product is supplied in secure, tamper-proof, export-grade packaging with complete regulatory documentation, making it suitable for oncology clinics, tertiary care hospitals, government cancer programs, and international pharmaceutical distributors.

Xbira 500 Tablets
Composition: Abiraterone Acetate 500 mg
International Trade Name: Zytiga®

Xbira 500 Tablets are a high-quality formulation of Abiraterone Acetate 500 mg, a selective androgen biosynthesis inhibitor, and a generic equivalent of the internationally recognized product marketed under the brand name Zytiga®. Manufactured in WHO-GMP certified facilities, Xbira Tablets are supplied by trusted pharmaceutical exporters from India to support advanced global oncology treatment programs, particularly in the management of prostate cancer.

Abiraterone acetate works by selectively inhibiting the CYP17 enzyme (17α-hydroxylase/C17,20-lyase), which is essential for androgen production. By suppressing androgen synthesis in the testes, adrenal glands, and tumor tissue, Xbira 500 helps reduce circulating testosterone levels, thereby slowing tumor growth and disease progression. This targeted hormonal therapy is typically administered in combination with prednisone or prednisolone.

Xbira 500 mg Tablets are primarily indicated for the treatment of metastatic castration-resistant prostate cancer (mCRPC) and metastatic hormone-sensitive prostate cancer (mHSPC), especially in patients who are receiving or have progressed on androgen deprivation therapy (ADT).

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Xbira Tablets are manufactured under stringent GMP and international pharmaceutical quality standards, ensuring consistent potency, safety, and long-term stability. The product is supplied in secure, tamper-proof, export-grade packaging with complete regulatory documentation, making it suitable for oncology clinics, tertiary care hospitals, government cancer programs, and international pharmaceutical distributors.

Azel 160 mg Tablets
Composition: Enzalutamide 160 mg
International Trade Name: Xtandi®

Azel 160 mg Tablets are a high-quality formulation of Enzalutamide, a non-steroidal androgen receptor signaling inhibitor, and a generic equivalent of the internationally recognized product marketed under the brand name Xtandi®. Manufactured in WHO-GMP certified facilities, Azel Tablets are supplied by trusted pharmaceutical exporters from India to support advanced global oncology treatment programs, particularly in the management of advanced and metastatic prostate cancer.

Enzalutamide works by blocking multiple steps in the androgen receptor signaling pathway, including androgen binding, nuclear translocation, and DNA transcription. By effectively inhibiting these mechanisms, Azel 160 mg helps prevent prostate cancer cell proliferation and slows disease progression, even in patients resistant to conventional androgen deprivation therapy (ADT).

Azel 160 mg Tablets are primarily indicated for the treatment of metastatic castration-resistant prostate cancer (mCRPC), non-metastatic castration-resistant prostate cancer (nmCRPC), and metastatic hormone-sensitive prostate cancer (mHSPC). They can be prescribed as monotherapy or in combination with ongoing ADT.

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Azel Tablets are manufactured under stringent GMP and international pharmaceutical quality standards, ensuring consistent efficacy, safety, and long-term stability. The product is supplied in secure, tamper-proof, export-grade packaging with complete regulatory documentation, making it suitable for oncology clinics, tertiary care hospitals, government cancer programs, and international pharmaceutical distributors.

Enzamide 40 mg Capsules
Composition: Enzalutamide 40 mg
International Trade Name: Xtandi®

Enzamide 40 mg Capsules are a high-quality formulation of Enzalutamide, a generic equivalent of the internationally recognized androgen receptor signaling inhibitor marketed under the brand name Xtandi®. Manufactured in WHO-GMP certified facilities, Enzamide is supplied by trusted pharmaceutical exporters from India to support advanced global oncology treatment programs, particularly in the management of advanced and metastatic prostate cancer.

Enzalutamide is a potent, non-steroidal androgen receptor inhibitor that blocks multiple steps in the androgen receptor signaling pathway, including androgen binding, nuclear translocation, and DNA transcription. By effectively inhibiting these mechanisms, Enzamide 40 helps prevent prostate cancer cell growth and proliferation, even in patients resistant to conventional androgen deprivation therapy.

Enzamide 40 mg Capsules are primarily indicated for the treatment of metastatic castration-resistant prostate cancer (mCRPC), non-metastatic castration-resistant prostate cancer (nmCRPC), and metastatic hormone-sensitive prostate cancer (mHSPC). They can be prescribed as monotherapy or in combination with ongoing androgen deprivation therapy (ADT).

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Enzamide is manufactured under stringent GMP and international pharmaceutical quality standards, ensuring consistent efficacy, safety, and long-term stability. The product is supplied in secure, tamper-proof, export-grade packaging with complete regulatory documentation, making it suitable for oncology clinics, tertiary care hospitals, government cancer programs, and international pharmaceutical distributors.

Enzandro 160 mg Tablets
Composition: Enzalutamide 160 mg
International Trade Name: Xtandi®

Enzandro 160 mg Tablets are a high-quality formulation of Enzalutamide, a non-steroidal androgen receptor signaling inhibitor, and a generic equivalent of the internationally recognized product marketed under the brand name Xtandi®. Manufactured in WHO-GMP certified facilities, Enzandro is supplied by trusted pharmaceutical exporters from India to support advanced global oncology treatment programs, particularly in the management of advanced and metastatic prostate cancer.

Enzalutamide works by blocking multiple steps in the androgen receptor signaling pathway, including androgen binding, nuclear translocation, and DNA transcription. By effectively inhibiting these mechanisms, Enzandro 160 mg helps prevent prostate cancer cell proliferation and slows disease progression, even in patients resistant to conventional androgen deprivation therapy (ADT).

Enzandro 160 mg Tablets are primarily indicated for the treatment of metastatic castration-resistant prostate cancer (mCRPC), non-metastatic castration-resistant prostate cancer (nmCRPC), and metastatic hormone-sensitive prostate cancer (mHSPC). They can be prescribed as monotherapy or in combination with ongoing ADT.

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Enzandro Tablets are manufactured under stringent GMP and international pharmaceutical quality standards, ensuring consistent efficacy, safety, and long-term stability. The product is supplied in secure, tamper-proof, export-grade packaging with complete regulatory documentation, making it suitable for oncology clinics, tertiary care hospitals, government cancer programs, and international pharmaceutical distributors.

Enzaneal 40 mg Capsules/Tablets
Composition: Enzalutamide 40 mg
International Trade Name: Xtandi®

Enzaneal 40 is a high-quality Enzalutamide 40 mg formulation, a generic equivalent of the internationally recognized androgen receptor signaling inhibitor marketed under the brand name Xtandi®. Manufactured in WHO-GMP certified facilities, Enzaneal is supplied by trusted pharmaceutical exporters from India to support advanced global oncology treatment programs, particularly in the management of advanced and metastatic prostate cancer.

Enzalutamide is a potent, non-steroidal androgen receptor inhibitor that blocks multiple steps in the androgen receptor signaling pathway, including androgen binding, nuclear translocation, and DNA transcription. By effectively inhibiting these mechanisms, Enzaneal 40 helps prevent prostate cancer cell growth and proliferation, even in patients resistant to conventional androgen deprivation therapy.

Enzaneal 40 mg is primarily indicated for the treatment of metastatic castration-resistant prostate cancer (mCRPC), non-metastatic castration-resistant prostate cancer (nmCRPC), and metastatic hormone-sensitive prostate cancer (mHSPC). It can be prescribed as monotherapy or in combination with ongoing androgen deprivation therapy (ADT).

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Enzaneal is manufactured under stringent GMP and international pharmaceutical quality standards, ensuring consistent efficacy, safety, and long-term stability. The product is supplied in secure, tamper-proof, export-grade packaging with complete regulatory documentation, making it suitable for oncology clinics, tertiary care hospitals, government cancer programs, and international pharmaceutical distributors.

Xylutide 40 mg Capsules
Composition: Enzalutamide 40 mg
International Trade Name: Xtandi®

Xylutide 40 mg Capsules are a high-quality formulation of Enzalutamide, a non-steroidal androgen receptor inhibitor, and a generic equivalent of the internationally recognized product marketed under the brand name Xtandi®. Manufactured in WHO-GMP certified facilities, Xylutide is supplied by trusted pharmaceutical exporters from India to support advanced global oncology treatment programs, particularly in the management of advanced and metastatic prostate cancer.

Enzalutamide works by blocking multiple steps in the androgen receptor signaling pathway, including androgen binding, nuclear translocation, and DNA transcription. By inhibiting these mechanisms, Xylutide 40 mg helps prevent prostate cancer cell proliferation and slows disease progression, even in patients resistant to conventional androgen deprivation therapy (ADT).

Xylutide 40 mg Capsules are primarily indicated for the treatment of metastatic castration-resistant prostate cancer (mCRPC), non-metastatic castration-resistant prostate cancer (nmCRPC), and metastatic hormone-sensitive prostate cancer (mHSPC). It can be prescribed as monotherapy or in combination with ongoing androgen deprivation therapy.

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Xylutide is manufactured under stringent GMP and international pharmaceutical quality standards, ensuring consistent efficacy, safety, and long-term stability. The product is supplied in secure, tamper-proof, export-grade packaging with complete regulatory documentation, making it suitable for oncology clinics, tertiary care hospitals, government cancer programs, and international pharmaceutical distributors.

Enzalieva 40mg Capsules/Tablets
Composition: Enzalutamide 40 mg
International Trade Name: Xtandi®

Enzalieva 40 is a high-quality Enzalutamide 40 mg formulation, a generic equivalent of the internationally recognized androgen receptor inhibitor marketed under the brand name Xtandi®. Manufactured in WHO-GMP certified facilities, Enzalieva is supplied by trusted pharmaceutical exporters from India to support advanced global oncology treatment programs, particularly in prostate cancer management.

Enzalutamide is a next-generation androgen receptor signaling inhibitor that blocks multiple steps in the androgen receptor pathway, including androgen binding, nuclear translocation, and DNA interaction. By effectively suppressing androgen-driven tumor growth, Enzalieva 40 helps slow disease progression and improve clinical outcomes in patients with advanced prostate cancer.

Enzalieva 40 mg is primarily indicated for the treatment of metastatic castration-resistant prostate cancer (mCRPC) and metastatic hormone-sensitive prostate cancer (mHSPC). It is commonly prescribed for patients who have progressed on or are receiving androgen deprivation therapy (ADT), offering a potent oral alternative to conventional chemotherapy.

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Enzalieva 40 is manufactured under stringent GMP and international pharmaceutical quality standards, ensuring consistent potency, safety, and long-term stability. The product is supplied in secure, tamper-proof, export-grade packaging with complete regulatory documentation, making it suitable for oncology clinics, tertiary care hospitals, government cancer programs, and international pharmaceutical distributors.

Enzabuzz 40 mg Capsules/Tablets
Composition: Enzalutamide 40 mg
International Trade Name: Xtandi®

Enzabuzz 40 is a high-quality Enzalutamide 40 mg formulation, a generic equivalent of the internationally recognized androgen receptor signaling inhibitor marketed under the brand name Xtandi®. Manufactured in WHO-GMP certified facilities, Enzabuzz is supplied by trusted pharmaceutical exporters from India to support advanced global oncology treatment programs, particularly in the management of advanced and metastatic prostate cancer.

Enzalutamide is a potent, non-steroidal androgen receptor inhibitor that blocks multiple steps in the androgen receptor signaling pathway, including androgen binding, nuclear translocation, and DNA transcription. By effectively inhibiting these mechanisms, Enzabuzz 40 helps prevent prostate cancer cell growth and proliferation, even in cases resistant to conventional androgen deprivation therapy.

Enzabuzz 40 mg is primarily indicated for the treatment of metastatic castration-resistant prostate cancer (mCRPC), non-metastatic castration-resistant prostate cancer (nmCRPC), and metastatic hormone-sensitive prostate cancer (mHSPC). It is typically prescribed as monotherapy or in combination with ongoing androgen deprivation therapy (ADT).

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Enzabuzz is manufactured under stringent GMP and international pharmaceutical quality standards, ensuring consistent efficacy, safety, and long-term stability. The product is supplied in secure, tamper-proof, export-grade packaging with complete regulatory documentation, making it suitable for oncology clinics, tertiary care hospitals, government cancer programs, and international pharmaceutical distributors.

Azel 40 mg Capsules
Composition: Enzalutamide 40 mg
International Trade Name: Xtandi®

Azel 40 mg Capsules are a high-quality formulation of Enzalutamide, a non-steroidal androgen receptor signaling inhibitor, and a generic equivalent of the internationally recognized product marketed under the brand name Xtandi®. Manufactured in WHO-GMP certified facilities, Azel Capsules are supplied by trusted pharmaceutical exporters from India to support advanced global oncology treatment programs, particularly in the management of advanced and metastatic prostate cancer.

Enzalutamide works by blocking multiple steps in the androgen receptor signaling pathway, including androgen binding, nuclear translocation, and DNA transcription. By effectively inhibiting these mechanisms, Azel 40 mg helps prevent prostate cancer cell proliferation and slows disease progression, even in patients resistant to conventional androgen deprivation therapy (ADT).

Azel 40 mg Capsules are primarily indicated for the treatment of metastatic castration-resistant prostate cancer (mCRPC), non-metastatic castration-resistant prostate cancer (nmCRPC), and metastatic hormone-sensitive prostate cancer (mHSPC). They can be prescribed as monotherapy or in combination with ongoing ADT.

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Azel Capsules are manufactured under stringent GMP and international pharmaceutical quality standards, ensuring consistent efficacy, safety, and long-term stability. The product is supplied in secure, tamper-proof, export-grade packaging with complete regulatory documentation, making it suitable for oncology clinics, tertiary care hospitals, government cancer programs, and international pharmaceutical distributors.

APNAT 60 mg Tablets
Composition: Apalutamide 60 mg
International Trade Name: Erleada®

APNAT 60 mg Tablets are a high-quality formulation of Apalutamide, a non-steroidal androgen receptor inhibitor, and a generic equivalent of the internationally recognized product marketed under the brand name Erleada®. Manufactured in WHO-GMP certified facilities, APNAT Tablets are supplied by trusted pharmaceutical exporters from India to support advanced global oncology treatment programs, particularly in the management of prostate cancer.

Apalutamide works by binding to androgen receptors and inhibiting androgen-driven signaling pathways, thereby preventing the growth and proliferation of prostate cancer cells. This targeted therapy is effective in slowing disease progression in patients with castration-resistant and non-metastatic prostate cancer.

APNAT 60 mg Tablets are primarily indicated for the treatment of non-metastatic castration-resistant prostate cancer (nmCRPC) and may also be used in selected patients with metastatic hormone-sensitive prostate cancer (mHSPC) as part of combination therapy.

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APNAT Tablets are manufactured under stringent GMP and international pharmaceutical quality standards, ensuring consistent efficacy, safety, and long-term stability. The product is supplied in secure, tamper-proof, export-grade packaging with complete regulatory documentation, making it suitable for oncology clinics, tertiary care hospitals, government cancer programs, and international pharmaceutical distributors.

Ibyra 100 mg Tablets
Composition: Olaparib 100 mg
International Trade Name: Lynparza®

Ibyra 100 mg Tablets are a high-quality formulation of Olaparib, a potent poly (ADP-ribose) polymerase (PARP) inhibitor, and a generic equivalent of the internationally recognized product marketed under the brand name Lynparza®. Manufactured in WHO-GMP certified facilities, Ibyra is supplied by trusted pharmaceutical exporters from India to support advanced global oncology treatment programs, particularly in the management of BRCA-mutated cancers.

Olaparib works by inhibiting the PARP enzyme, which plays a critical role in DNA repair in cancer cells. By blocking DNA repair mechanisms, Ibyra induces cancer cell death, especially in tumors with BRCA1 or BRCA2 mutations, making it an effective targeted therapy for patients with specific genetic profiles.

Ibyra 100 mg Tablets are primarily indicated for the treatment of BRCA-mutated ovarian cancer, breast cancer, pancreatic cancer, and prostate cancer, either as monotherapy or as maintenance therapy following response to platinum-based chemotherapy.

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Ibyra Tablets are manufactured under stringent GMP and international pharmaceutical quality standards, ensuring consistent potency, safety, and long-term stability. The product is supplied in secure, tamper-proof, export-grade packaging with complete regulatory documentation, making it suitable for oncology clinics, tertiary care hospitals, government cancer programs, and international pharmaceutical distributors.

Ribaxa 150 mg Tablets
Composition: Olaparib 150 mg
International Trade Name: Lynparza®

Ribaxa 150 mg Tablets are a high-quality formulation of Olaparib, a potent poly (ADP-ribose) polymerase (PARP) inhibitor, and a generic equivalent of the internationally recognized product marketed under the brand name Lynparza®. Manufactured in WHO-GMP certified facilities, Ribaxa is supplied by trusted pharmaceutical exporters from India to support advanced global oncology treatment programs, particularly in the management of BRCA-mutated cancers.

Olaparib works by inhibiting the PARP enzyme, which plays a critical role in DNA repair in cancer cells. By blocking DNA repair mechanisms, Ribaxa induces apoptosis in cancer cells, especially in tumors with BRCA1 or BRCA2 mutations, making it an effective targeted therapy for patients with specific genetic profiles.

Ribaxa 150 mg Tablets are primarily indicated for the treatment of BRCA-mutated ovarian cancer, breast cancer, pancreatic cancer, and prostate cancer, either as monotherapy or as maintenance therapy following response to platinum-based chemotherapy.

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Ribaxa Tablets are manufactured under stringent GMP and international pharmaceutical quality standards, ensuring consistent potency, safety, and long-term stability. The product is supplied in secure, tamper-proof, export-grade packaging with complete regulatory documentation, making it suitable for oncology clinics, tertiary care hospitals, government cancer programs, and international pharmaceutical distributors.

Parbraze 150 mg Tablets
Composition: Olaparib 150 mg
International Trade Name: Lynparza®

Parbraze 150 mg Tablets are a high-quality formulation of Olaparib, a potent poly (ADP-ribose) polymerase (PARP) inhibitor, and a generic equivalent of the internationally recognized product marketed under the brand name Lynparza®. Manufactured in WHO-GMP certified facilities, Parbraze is supplied by trusted pharmaceutical exporters from India to support advanced global oncology treatment programs, particularly in the management of BRCA-mutated cancers.

Olaparib works by inhibiting the PARP enzyme, which plays a critical role in DNA repair in cancer cells. By blocking DNA repair mechanisms, Parbraze induces apoptosis in cancer cells, especially in tumors with BRCA1 or BRCA2 mutations, making it an effective targeted therapy for patients with specific genetic profiles.

Parbraze 150 mg Tablets are primarily indicated for the treatment of BRCA-mutated ovarian cancer, breast cancer, pancreatic cancer, and prostate cancer, either as monotherapy or as maintenance therapy following response to platinum-based chemotherapy.

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Parbraze Tablets are manufactured under stringent GMP and international pharmaceutical quality standards, ensuring consistent potency, safety, and long-term stability. The product is supplied in secure, tamper-proof, export-grade packaging with complete regulatory documentation, making it suitable for oncology clinics, tertiary care hospitals, government cancer programs, and international pharmaceutical distributors.

OLANAMO 150 mg Tablets
Composition: Olaparib 150 mg
International Trade Name: Lynparza®

OLANAMO 150 mg Tablets are a high-quality formulation of Olaparib, a potent poly (ADP-ribose) polymerase (PARP) inhibitor, and a generic equivalent of the internationally recognized product marketed under the brand name Lynparza®. Manufactured in WHO-GMP certified facilities, OLANAMO is supplied by trusted pharmaceutical exporters from India to support advanced global oncology treatment programs, particularly in the management of BRCA-mutated cancers.

Olaparib works by inhibiting the PARP enzyme, which is essential for DNA repair in cancer cells. By blocking DNA repair mechanisms, OLANAMO induces apoptosis in cancer cells, especially in tumors with BRCA1 or BRCA2 mutations, making it an effective targeted therapy for patients with specific genetic profiles.

OLANAMO 150 mg Tablets are primarily indicated for the treatment of BRCA-mutated ovarian cancer, breast cancer, pancreatic cancer, and prostate cancer, either as monotherapy or as maintenance therapy following response to platinum-based chemotherapy.

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OLANAMO Tablets are manufactured under stringent GMP and international pharmaceutical quality standards, ensuring consistent potency, safety, and long-term stability. The product is supplied in secure, tamper-proof, export-grade packaging with complete regulatory documentation, making it suitable for oncology clinics, tertiary care hospitals, government cancer programs, and international pharmaceutical distributors.

Olabir 150mg Tablets
Composition: Olaparib Tablets 150mg
International Trade Name: Lynparza®

Olabir 150 is a high-quality Olaparib Tablets 150mg, a generic equivalent of the internationally recognized PARP inhibitor marketed under the brand name Lynparza®. Manufactured in WHO-GMP certified facilities, Olabir Tablets are supplied by trusted pharmaceutical manufacturers and exporters from India to support advanced global oncology treatment programs.

Olaparib is a targeted poly (ADP-ribose) polymerase (PARP) inhibitor that exploits defects in DNA repair pathways, particularly in BRCA-mutated and homologous recombination–deficient (HRD) cancers, leading to selective cancer cell death. Olabir 150mg Tablets are primarily indicated for the treatment of ovarian cancer, breast cancer, prostate cancer, and pancreatic cancer, either as monotherapy or maintenance therapy following platinum-based chemotherapy, as per approved clinical guidelines.

Olabir Olaparib Tablets 150mg are widely used in oncology hospitals, cancer specialty centers, and government oncology programs due to their proven efficacy, oral convenience, and compatibility with international treatment protocols.

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Olabir 150 Olaparib Tablets are manufactured under stringent GMP and international pharmaceutical quality standards, ensuring consistent potency, bioavailability, and long-term stability. The product is supplied in secure, tamper-evident, export-grade packaging with complete regulatory and quality documentation, making it suitable for international pharmaceutical distributors, oncology clinics, hospitals, and institutional cancer treatment programs worldwide.

Luprova 22.5 mg Depot Injection
Composition: Leuprolide Acetate 22.5 mg
International Trade Name: Lupron®

Luprova 22.5 mg Depot Injection is a high-quality, long-acting formulation of Leuprolide Acetate, a synthetic gonadotropin-releasing hormone (GnRH) agonist, and a generic equivalent of the internationally recognized product marketed under the brand name Lupron®. Manufactured in WHO-GMP certified facilities, Luprova is supplied by trusted pharmaceutical exporters from India to support advanced global oncology and hormone therapy programs, particularly in the management of prostate cancer and other hormone-sensitive conditions.

Leuprolide acetate works by initially stimulating and then downregulating pituitary GnRH receptors, leading to suppression of luteinizing hormone (LH) and follicle-stimulating hormone (FSH). This results in a significant reduction of testosterone in men and estrogen in women, providing effective hormone therapy for conditions such as advanced prostate cancer, endometriosis, uterine fibroids, and assisted reproduction protocols.

Luprova 22.5 mg Depot Injection is primarily indicated for advanced prostate cancer, endometriosis, uterine fibroids, and other hormone-dependent conditions requiring sustained hormone suppression over a 3-month period.

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Luprova is manufactured under stringent GMP and international pharmaceutical quality standards, ensuring consistent efficacy, safety, and long-term stability. The injection is supplied in secure, tamper-proof, export-grade packaging with complete regulatory documentation, making it suitable for oncology clinics, tertiary care hospitals, government cancer programs, and international pharmaceutical distributors.

Ahabir 500 mg Tablets
Composition: Abiraterone Acetate 500 mg Tablets
International Trade Name: Zytiga®

Ahabir 500 is a high-quality Abiraterone Acetate 500 mg tablet, a generic equivalent of the internationally recognized androgen biosynthesis inhibitor marketed under the brand name Zytiga®. Manufactured in WHO-GMP certified facilities, Ahabir Tablets are supplied by trusted pharmaceutical exporters from India to support advanced global oncology treatment programs, particularly in the treatment of prostate cancer.

Abiraterone acetate is a potent, selective inhibitor of the CYP17 enzyme (17α-hydroxylase/C17,20-lyase), which plays a critical role in androgen production. By suppressing androgen synthesis in the testes, adrenal glands, and tumor tissue, Ahabir 500 helps significantly reduce testosterone levels, thereby slowing tumor growth and disease progression. This targeted hormonal therapy is typically administered in combination with prednisone or prednisolone.

Ahabir 500 mg Tablets are primarily indicated for the treatment of metastatic castration-resistant prostate cancer (mCRPC) and metastatic hormone-sensitive prostate cancer (mHSPC), especially in patients who are receiving or have progressed on androgen deprivation therapy (ADT).

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Ahabir Tablets are manufactured under stringent GMP and international pharmaceutical quality standards, ensuring consistent potency, safety, and long-term stability. The product is supplied in secure, tamper-proof, export-grade packaging with complete regulatory documentation, making it suitable for oncology clinics, tertiary care hospitals, government cancer programs, and international pharmaceutical distributors.

Enzalutamide 80 mg Tablets
Composition: Enzalutamide 80 mg
International Trade Name: Xtandi®

Enzalutamide 80 mg Tablets are a high-quality formulation of Enzalutamide, a generic equivalent of the internationally recognized androgen receptor signaling inhibitor marketed under the brand name Xtandi®. Manufactured in WHO-GMP certified facilities, these tablets are supplied by trusted pharmaceutical exporters from India to support advanced global oncology treatment programs, particularly in the management of advanced and metastatic prostate cancer.

Enzalutamide is a potent, non-steroidal androgen receptor inhibitor that blocks multiple steps in the androgen receptor signaling pathway, including androgen binding, nuclear translocation, and DNA transcription. By inhibiting these mechanisms, Enzalutamide 80 mg helps prevent prostate cancer cell growth and proliferation, even in patients resistant to conventional androgen deprivation therapy.

These tablets are primarily indicated for the treatment of metastatic castration-resistant prostate cancer (mCRPC), non-metastatic castration-resistant prostate cancer (nmCRPC), and metastatic hormone-sensitive prostate cancer (mHSPC). Enzalutamide can be prescribed as monotherapy or alongside ongoing androgen deprivation therapy (ADT).

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Enzalutamide 80 mg Tablets are manufactured under stringent GMP and international pharmaceutical quality standards, ensuring consistent efficacy, safety, and long-term stability. The product is supplied in secure, tamper-proof, export-grade packaging with complete regulatory documentation, making it suitable for oncology clinics, tertiary care hospitals, government cancer programs, and international pharmaceutical distributors.

Bracanat 150 mg Tablets
Composition: Olaparib 150 mg
International Trade Name: Lynparza®

Bracanat 150 mg Tablets are a high-quality formulation of Olaparib, a potent poly (ADP-ribose) polymerase (PARP) inhibitor, and a generic equivalent of the internationally recognized product marketed under the brand name Lynparza®. Manufactured in WHO-GMP certified facilities, Bracanat is supplied by trusted pharmaceutical exporters from India to support advanced global oncology treatment programs, particularly in the management of BRCA-mutated cancers.

Olaparib works by inhibiting the PARP enzyme, which plays a critical role in DNA repair in cancer cells. By blocking DNA repair mechanisms, Bracanat induces apoptosis in cancer cells, especially in tumors with BRCA1 or BRCA2 mutations, making it an effective targeted therapy for patients with specific genetic profiles.

Bracanat 150 mg Tablets are primarily indicated for the treatment of BRCA-mutated ovarian cancer, breast cancer, pancreatic cancer, and prostate cancer, either as monotherapy or as maintenance therapy following response to platinum-based chemotherapy.

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Bracanat Tablets are manufactured under stringent GMP and international pharmaceutical quality standards, ensuring consistent potency, safety, and long-term stability. The product is supplied in secure, tamper-proof, export-grade packaging with complete regulatory documentation, making it suitable for oncology clinics, tertiary care hospitals, government cancer programs, and international pharmaceutical distributors.

Tesprolix 120 mg Tablets
Composition: Relugolix 120 mg
International Trade Name: Orgovyx®

Tesprolix 120 mg Tablets are a high-quality formulation of Relugolix, a potent oral gonadotropin-releasing hormone (GnRH) receptor antagonist, and a generic equivalent of the internationally recognized product marketed under the brand name Orgovyx®. Manufactured in WHO-GMP certified facilities, Tesprolix is supplied by trusted pharmaceutical exporters from India to support advanced global oncology treatment programs, particularly in the management of advanced prostate cancer.

Relugolix works by directly inhibiting GnRH receptors in the pituitary gland, leading to rapid suppression of luteinizing hormone (LH) and follicle-stimulating hormone (FSH), which in turn reduces testosterone production. This mechanism provides effective androgen deprivation therapy without the initial testosterone surge associated with traditional GnRH agonists.

Tesprolix 120 mg Tablets are primarily indicated for the treatment of advanced prostate cancer, metastatic hormone-sensitive prostate cancer (mHSPC), and as part of androgen deprivation therapy in patients requiring sustained testosterone suppression.

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Tesprolix Tablets are manufactured under stringent GMP and international pharmaceutical quality standards, ensuring consistent potency, safety, and long-term stability. The product is supplied in secure, tamper-proof, export-grade packaging with complete regulatory documentation, making it suitable for oncology clinics, tertiary care hospitals, government cancer programs, and international pharmaceutical distributors.

AB-TYRA 500 Tablets
Composition: Abiraterone Acetate 500 mg Tablets
International Trade Name: Zytiga®

AB-TYRA 500 is a high-quality Abiraterone Acetate 500 mg tablet, a generic equivalent of the internationally recognized androgen biosynthesis inhibitor marketed under the brand name Zytiga®. Manufactured in WHO-GMP certified facilities, AB-TYRA Tablets are supplied by trusted pharmaceutical exporters from India to support advanced global oncology treatment programs, particularly in the management of prostate cancer.

Abiraterone acetate is a potent, selective inhibitor of the CYP17 enzyme (17α-hydroxylase/C17,20-lyase), which plays a critical role in androgen production. By suppressing androgen synthesis in the testes, adrenal glands, and tumor tissue, AB-TYRA 500 helps reduce circulating testosterone levels, thereby slowing tumor growth and disease progression. This targeted hormonal therapy is typically administered in combination with prednisone or prednisolone.

AB-TYRA 500 mg Tablets are primarily indicated for the treatment of metastatic castration-resistant prostate cancer (mCRPC) and metastatic hormone-sensitive prostate cancer (mHSPC), especially in patients who are receiving or have progressed on androgen deprivation therapy (ADT).

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AB-TYRA Tablets are manufactured under stringent GMP and international pharmaceutical quality standards, ensuring consistent potency, safety, and long-term stability. The product is supplied in secure, tamper-proof, export-grade packaging with complete regulatory documentation, making it suitable for oncology clinics, tertiary care hospitals, government cancer programs, and international pharmaceutical distributors.

AB-TYRA 250 mg Tablets
Composition: Abiraterone Acetate 250 mg Tablets IP
International Trade Name: Zytiga®

AB-TYRA 250 is a high-quality Abiraterone Acetate 250 mg tablet, a generic equivalent of the internationally recognized androgen biosynthesis inhibitor marketed under the brand name Zytiga®. Manufactured in WHO-GMP certified facilities, AB-TYRA Tablets are supplied by trusted pharmaceutical exporters from India to support advanced global oncology treatment programs, particularly in the management of prostate cancer.

Abiraterone acetate is a potent, selective inhibitor of the CYP17 enzyme (17α-hydroxylase/C17,20-lyase), which is critical in androgen production. By suppressing androgen synthesis in the testes, adrenal glands, and tumor tissue, AB-TYRA 250 helps reduce testosterone levels and slow tumor growth and disease progression. This targeted hormonal therapy is typically administered in combination with prednisone or prednisolone.

AB-TYRA 250 mg Tablets are primarily indicated for the treatment of metastatic castration-resistant prostate cancer (mCRPC) and metastatic hormone-sensitive prostate cancer (mHSPC), especially in patients who are receiving or have progressed on androgen deprivation therapy (ADT).

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AB-TYRA Tablets are manufactured under stringent GMP and international pharmaceutical quality standards, ensuring consistent potency, safety, and long-term stability. The product is supplied in secure, tamper-proof, export-grade packaging with complete regulatory documentation, making it suitable for oncology clinics, tertiary care hospitals, government cancer programs, and international pharmaceutical distributors.

OLAPYRA 150 Tablets
Composition: Olaparib 150 mg
International Trade Name: Lynparza®

OLAPYRA 150 mg Tablets are a high-quality formulation of Olaparib, a potent poly (ADP-ribose) polymerase (PARP) inhibitor, and a generic equivalent of the internationally recognized product marketed under the brand name Lynparza®. Manufactured in WHO-GMP certified facilities, OLAPYRA is supplied by trusted pharmaceutical exporters from India to support advanced global oncology treatment programs, particularly in the management of BRCA-mutated cancers.

Olaparib works by inhibiting the PARP enzyme, which plays a critical role in DNA repair in cancer cells. By blocking DNA repair mechanisms, OLAPYRA induces apoptosis in cancer cells, especially in tumors with BRCA1 or BRCA2 mutations, making it an effective targeted therapy for patients with specific genetic profiles.

OLAPYRA 150 mg Tablets are primarily indicated for the treatment of BRCA-mutated ovarian cancer, breast cancer, pancreatic cancer, and prostate cancer, either as monotherapy or as maintenance therapy following response to platinum-based chemotherapy.

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OLAPYRA Tablets are manufactured under stringent GMP and international pharmaceutical quality standards, ensuring consistent potency, safety, and long-term stability. The product is supplied in secure, tamper-proof, export-grade packaging with complete regulatory documentation, making it suitable for oncology clinics, tertiary care hospitals, government cancer programs, and international pharmaceutical distributors.

ABIRALIEVA Tablets
Composition: Abiraterone Acetate Tablets (250 mg / 500 mg – as applicable)
International Trade Name: Zytiga®

ABIRALIEVA is a high-quality Abiraterone Acetate formulation, a generic equivalent of the internationally recognized androgen biosynthesis inhibitor marketed under the brand name Zytiga®. Manufactured in WHO-GMP certified facilities, ABIRALIEVA Tablets are supplied by trusted pharmaceutical exporters from India to support advanced global oncology treatment programs, particularly in prostate cancer therapy.

Abiraterone acetate is a selective inhibitor of the CYP17 enzyme, which plays a crucial role in androgen production. By blocking androgen synthesis in the testes, adrenal glands, and tumor tissues, ABIRALIEVA helps reduce circulating androgen levels, thereby slowing tumor growth and disease progression in hormone-dependent prostate cancer.

ABIRALIEVA is primarily indicated for the treatment of metastatic castration-resistant prostate cancer (mCRPC) and metastatic hormone-sensitive prostate cancer (mHSPC). It is commonly administered in combination with prednisone or prednisolone as part of a comprehensive hormonal therapy regimen.

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Abiralieva 500mg Tablets
Composition: Abiraterone Acetate 500 mg Tablets
International Trade Name: Zytiga®

Abiralieva 500 is a high-quality Abiraterone Acetate 500 mg tablet, a generic equivalent of the internationally recognized androgen biosynthesis inhibitor marketed under the brand name Zytiga®. Manufactured in WHO-GMP certified facilities, Abiralieva Tablets are supplied by trusted pharmaceutical exporters from India to support advanced global oncology treatment programs, particularly in prostate cancer management.

Abiraterone acetate is a potent, selective inhibitor of CYP17 (17α-hydroxylase/C17,20-lyase), a critical enzyme involved in androgen production. By suppressing androgen synthesis in the testes, adrenal glands, and tumor tissue, Abiralieva 500 mg Tablets help reduce tumor growth and disease progression in hormone-driven prostate cancer. This targeted hormonal therapy is commonly administered alongside prednisone or prednisolone.

Abiralieva 500 mg is primarily indicated for the treatment of metastatic castration-resistant prostate cancer (mCRPC) and metastatic hormone-sensitive prostate cancer (mHSPC), especially in patients who have progressed on or are receiving androgen deprivation therapy (ADT).

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Abiralieva 500 Tablets are manufactured under stringent GMP and international pharmaceutical quality standards, ensuring consistent potency, safety, and long-term stability. The product is supplied in secure, tamper-proof, export-grade packaging with complete regulatory documentation, making it suitable for oncology clinics, tertiary care hospitals, government cancer programs, and international pharmaceutical distributors.

Taxonab 100 mg Injection
Composition: Paclitaxel 100 mg
International Trade Name: Taxol®

Taxonab 100 mg Injection is a high-quality formulation of Paclitaxel, a chemotherapeutic agent widely used in oncology, and a generic equivalent of the internationally recognized product marketed under the brand name Taxol®. Manufactured in WHO-GMP certified facilities, Taxonab Injection is supplied by trusted pharmaceutical exporters from India to support advanced global cancer treatment programs.

Paclitaxel is a mitotic inhibitor that works by stabilizing microtubules and preventing their depolymerization, thereby inhibiting cell division. By targeting rapidly dividing cancer cells, Taxonab 100 mg effectively slows tumor growth and progression across a variety of malignancies.

Taxonab 100 mg Injection is primarily indicated for the treatment of breast cancer, ovarian cancer, non-small cell lung cancer (NSCLC), Kaposi’s sarcoma, and other solid tumors, either as monotherapy or in combination with other chemotherapeutic agents, depending on clinical protocols.

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Taxonab 100 mg Injection is manufactured under stringent GMP and international pharmaceutical quality standards, ensuring consistent efficacy, safety, and long-term stability. The product is supplied in secure, tamper-proof, export-grade packaging with complete regulatory documentation, making it suitable for oncology infusion centers, tertiary care hospitals, government cancer programs, and international pharmaceutical distributors.

Dutaxel 100 mg Injection
Composition: Paclitaxel 100 mg
International Trade Name: Taxol®

Dutaxel 100 mg Injection is a high-quality formulation of Paclitaxel, a chemotherapeutic agent widely used in oncology, and a generic equivalent of the internationally recognized product marketed under the brand name Taxol®. Manufactured in WHO-GMP certified facilities, Dutaxel Injection is supplied by trusted pharmaceutical exporters from India to support advanced global cancer treatment programs.

Paclitaxel is a mitotic inhibitor that stabilizes microtubules and prevents their depolymerization, thereby inhibiting cell division. By targeting rapidly dividing cancer cells, Dutaxel 100 mg Injection effectively slows tumor growth and progression across a variety of malignancies.

Dutaxel 100 mg Injection is primarily indicated for the treatment of breast cancer, ovarian cancer, non-small cell lung cancer (NSCLC), Kaposi’s sarcoma, and other solid tumors, either as monotherapy or in combination with other chemotherapeutic agents, depending on clinical protocols.

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Dutaxel 100 mg Injection is manufactured under stringent GMP and international pharmaceutical quality standards, ensuring consistent efficacy, safety, and long-term stability. The product is supplied in secure, tamper-proof, export-grade packaging with complete regulatory documentation, making it suitable for oncology infusion centers, tertiary care hospitals, government cancer programs, and international pharmaceutical distributors.

Nanopacli 100 mg Injection
Composition: Paclitaxel 100 mg
International Trade Name: Taxol®

Nanopacli 100 mg Injection is a high-quality formulation of Paclitaxel, a potent chemotherapeutic agent, and a generic equivalent of the internationally recognized product marketed under the brand name Taxol®. Manufactured in WHO-GMP certified facilities, Nanopacli is supplied by trusted pharmaceutical exporters from India to support advanced global oncology treatment programs.

Paclitaxel is a microtubule-stabilizing agent that inhibits cancer cell division by preventing microtubule disassembly during mitosis. This mechanism effectively halts tumor growth and induces apoptosis, making Nanopacli a highly effective therapy against a wide range of solid tumors.

Nanopacli 100 mg Injection is primarily indicated for the treatment of breast cancer, ovarian cancer, non-small cell lung cancer (NSCLC), and other solid tumors where Paclitaxel therapy is indicated. The injection is administered intravenously under the supervision of an oncology specialist.

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Nanopacli is manufactured under stringent GMP and international pharmaceutical quality standards, ensuring consistent efficacy, safety, and long-term stability. The injection is supplied in secure, tamper-proof, export-grade packaging with complete regulatory documentation, making it suitable for oncology infusion centers, tertiary care hospitals, government cancer programs, and international pharmaceutical distributors.

Celtax 260 mg Injection
Composition: Paclitaxel 260 mg
International Trade Name: Taxol®

Celtax 260 mg Injection is a high-quality formulation of Paclitaxel, a potent chemotherapeutic agent, and a generic equivalent of the internationally recognized product marketed under the brand name Taxol®. Manufactured in WHO-GMP certified facilities, Celtax is supplied by trusted pharmaceutical exporters from India to support advanced global oncology treatment programs.

Paclitaxel works by stabilizing microtubules, preventing their disassembly during cell division, which halts mitosis and induces apoptosis in rapidly dividing cancer cells. This mechanism makes Celtax highly effective against a wide range of solid tumors.

Celtax 260 mg Injection is primarily indicated for the treatment of breast cancer, ovarian cancer, non-small cell lung cancer (NSCLC), and other solid tumors where Paclitaxel therapy is indicated. The injection is administered intravenously under the supervision of an oncology specialist.

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Celtax is manufactured under stringent GMP and international pharmaceutical quality standards, ensuring consistent efficacy, safety, and long-term stability. The injection is supplied in secure, tamper-proof, export-grade packaging with complete regulatory documentation, making it suitable for oncology infusion centers, tertiary care hospitals, government cancer programs, and international pharmaceutical distributors.

NAB Celtax Paclitaxel Injection
Composition: Paclitaxel 100 mg / 260 mg / 300 mg per vial (as per requirement)
International Trade Name: Taxol®

NAB Celtax is a high-quality formulation of Paclitaxel, a potent chemotherapeutic agent, and a generic equivalent of the internationally recognized product marketed under the brand name Taxol®. Manufactured in WHO-GMP certified facilities, NAB Celtax is supplied by trusted pharmaceutical exporters from India to support advanced global oncology treatment programs.

Paclitaxel works as a microtubule-stabilizing agent that inhibits cancer cell division by preventing microtubule disassembly during mitosis. This mechanism effectively halts tumor growth and induces apoptosis, making NAB Celtax a highly effective therapy for a wide range of solid tumors.

NAB Celtax Paclitaxel Injection is primarily indicated for the treatment of breast cancer, ovarian cancer, non-small cell lung cancer (NSCLC), and other solid tumors where Paclitaxel therapy is indicated. The injection is administered intravenously under the supervision of an oncology specialist.

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NAB Celtax is manufactured under stringent GMP and international pharmaceutical quality standards, ensuring consistent efficacy, safety, and long-term stability. The injection is supplied in secure, tamper-proof, export-grade packaging with complete regulatory documentation, making it suitable for oncology infusion centers, tertiary care hospitals, government cancer programs, and international pharmaceutical distributors.

Celtax 100 mg Injection
Composition: Paclitaxel 100 mg
International Trade Name: Taxol®

Celtax 100 mg Injection is a high-quality formulation of Paclitaxel, a potent chemotherapeutic agent, and a generic equivalent of the internationally recognized product marketed under the brand name Taxol®. Manufactured in WHO-GMP certified facilities, Celtax is supplied by trusted pharmaceutical exporters from India to support advanced global oncology treatment programs.

Paclitaxel works by stabilizing microtubules, preventing their disassembly during mitosis, thereby inhibiting cell division and inducing apoptosis in rapidly dividing cancer cells. This mechanism makes Celtax highly effective against a wide range of solid tumors.

Celtax 100 mg Injection is primarily indicated for the treatment of breast cancer, ovarian cancer, non-small cell lung cancer (NSCLC), and other solid tumors where Paclitaxel therapy is indicated. The injection is administered intravenously under the supervision of an oncology specialist.

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Celtax is manufactured under stringent GMP and international pharmaceutical quality standards, ensuring consistent efficacy, safety, and long-term stability. The injection is supplied in secure, tamper-proof, export-grade packaging with complete regulatory documentation, making it suitable for oncology infusion centers, tertiary care hospitals, government cancer programs, and international pharmaceutical distributors.

Mitotax 100 mg Injection
Composition: Paclitaxel 100 mg
International Trade Name: Taxol®

Mitotax 100 mg Injection is a high-quality formulation of Paclitaxel, a potent chemotherapeutic agent, and a generic equivalent of the internationally recognized product marketed under the brand name Taxol®. Manufactured in WHO-GMP certified facilities, Mitotax is supplied by trusted pharmaceutical exporters from India to support advanced global oncology treatment programs.

Paclitaxel is a microtubule-stabilizing agent that inhibits cancer cell division by preventing microtubule disassembly during mitosis. This mechanism effectively halts tumor growth and induces apoptosis, making Mitotax a highly effective therapy for a wide range of solid tumors.

Mitotax 100 mg Injection is primarily indicated for the treatment of breast cancer, ovarian cancer, non-small cell lung cancer (NSCLC), and other solid tumors where Paclitaxel therapy is indicated. The injection is administered intravenously under the supervision of an oncology specialist.

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Mitotax is manufactured under stringent GMP and international pharmaceutical quality standards, ensuring consistent efficacy, safety, and long-term stability. The injection is supplied in secure, tamper-proof, export-grade packaging with complete regulatory documentation, making it suitable for oncology infusion centers, tertiary care hospitals, government cancer programs, and international pharmaceutical distributors.