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Nifedipine

NDC 72162-2261 · HUMAN PRESCRIPTION DRUG · TABLET, EXTENDED RELEASE

Labeler / ManufacturerBryant Ranch Prepack
Marketing categoryAbbreviated NDA (generic) · App ANDA076070
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsNIFEDIPINE (90 mg/1)
Marketing started20020816
Package count1

External sources

Source: openFDA. Public-domain (CC0).