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Alembic Pharma gets USFDA nod for 2 generic products

The company has received approval from the United States Food and Drug Administration (USFDA) for its abbreviated new drug application (ANDA) for Teriflunomide tablets in the strengths of 7 mg and 14 mg, Alembic Pharmaceuticals said in a filing to BSE.

Original source: https://health.economictimes.indiatimes.com/news/pharma/alembic-pharma-gets-usfda-nod-for-2-generic-products/68988809?utm_source=RSS&utm_medium=ETRSS

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