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Nifedipine

NDC 62332-732 · HUMAN PRESCRIPTION DRUG · TABLET, EXTENDED RELEASE

Labeler / ManufacturerAlembic Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA216896
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsNIFEDIPINE (30 mg/1)
Marketing started20221123
Package count3

External sources

Source: openFDA. Public-domain (CC0).