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Alembic is a multi-product, multi-location enterprise that delivers a variety of complex chemistries for pharmaceutical companies worldwide. Learn about its history, business, products, research and development, and social responsibility.
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Manufacturing Facilities. Panelav Village Panelav, PO...
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Alembic Pharmaceuticals Limited is an Indian pharmaceutical...
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Alembic Pharmaceuticals, a pioneering company in Vadodara...
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Alembic Pharmaceuticals Is Pharmaceutical Products...
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Alembic Pharmaceuticals Limited Alembic Road, Vadodara – 390...
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Regular community intervention, ethical business practices...
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Alembic Pharmaceuticals Is Also An Api Manufacturers In...
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Alembic Pharmaceuticals is an Indian company with 110+ years of experience in the generics pharma industry. It produces and markets APIs, formulations, and international generics across the globe.
Alembic Pharmaceuticals Ltd. is an Indian multinational pharmaceutical company headquartered in Vadodara. [2] It is involved in the manufacture of pharmaceutical products, pharmaceutical substances and intermediates. It is also termed to be a market leader in macrolides segment of anti-infective drugs in India.
Alembic Pharmaceuticals is a leading generic pharma company in India with global presence. It produces formulations, generics and APIs with vertical integration capabilities. See its corporate history, vision and latest annual reports.
2 days ago · Mumbai: Alembic Pharmaceuticals Limited announced that it has received tentative approval from the US Food & Drug Administration (US FDA) for its abbreviated new drug application (ANDA) for ...
2 days ago · New Delhi: Alembic Pharmaceuticals on Thursday said it has received tentative approval from the US health regulator for its generic Ivosidenib tablets used in the treatment of certain types of cancer of bone marrow and bile duct. The tentative approval by the US Food & Drug Administration ( USFDA) is for the abbreviated new drug application ...
Alembic Pharmaceuticals Limited on Thursday announced that it has received tentative approval from the US Food & Drug Administration (USFDA) for its Abbreviated New Drug Application (ANDA) for ...
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