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Nifedipine

NDC 0904-7208 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Labeler / ManufacturerMajor Pharmaceuticals
Marketing categoryAbbreviated NDA (generic) · App ANDA203126
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsNIFEDIPINE (30 mg/1)
Marketing started20141101
Package count2

External sources

Source: openFDA. Public-domain (CC0).