US Food and Drug Administration (FDA) has given its nod to Indian pharmaceutical major Zydus Cadila for manufacturing of Mesalamine Delayed-Release Tablets...
Indian pharmaceutical company Natco Pharma Limited has received successful Establishment Inspection Report (EIR) from the US Food and Drug Administration (USFDA) for...
India has been doing exceptionally well in the pharmaceutical sector for the last 20-25 years, but since the country agreed to comply...
Glenmark Pharmaceuticals on Friday announced that the leading research“based global pharmaceutical company has been granted final Abbreviated New Drug Application (ANDA) approval...
Jubilant Pharma Limited, a subsidiary of Noida-based Jubilant Life Sciences Ltd, has received Abbreviated New Drug Application (ANDA) final approval for Bupropion...
Bengaluru-based Indian pharmaceutical major Strides Shasun has announced that the company has received approval from US Food and Drug Administration (USFDA) to...
Zydus Pharmaceuticals’ subsidiary Nesher Pharmaceuticals has recently received the final approval from US Food and Drug Administration (USFDA) to market Dextroamphetamine Sulfate...
Alembic Pharma, a leader in branded generics in India, has received the approval from the US Food and Drug Administration (USFDA) for...
Mumbai-headquartered pharma major Glenmark has entered into a licensing agreement with Advanced Proteome (AP) Therapeutics — a company co-founded by Indian-origin Vinod...
Indian pharmaceutical major Zydus Cadila has managed to receive the final approval from the US health regulator Food and Drug Administration (USFDA)...
Aurobindo Pharma Limited, one of the top Indian pharmaceutical companies, has received final approval from the US Food and Drug Administration (USFDA)...
Indian pharmaceutical major Zydus Cadila has received the final approval from the US Food and Drug Administration (USFDA) to market its anti-viral...
Zydus Cadila will start manufacturing anti-cholesterol tablet Ezetimibe from its plant in Moraiya, Ahmedabad, after getting approval from US Food and Drug...
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