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Nifedipine

NDC 62175-262 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Labeler / ManufacturerLannett Company, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA077127
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsNIFEDIPINE (90 mg/1)
Marketing started20071003
Package count3

External sources

Source: openFDA. Public-domain (CC0).