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Nifedipine

NDC 71205-965 · HUMAN PRESCRIPTION DRUG · TABLET, EXTENDED RELEASE

Labeler / ManufacturerProficient Rx LP
Marketing categoryAbbreviated NDA (generic) · App ANDA203126
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsNIFEDIPINE (90 mg/1)
Marketing started20141101
Package count9

External sources

Source: openFDA. Public-domain (CC0).