FDA NDC Directory · JSON-LD · Markdown

NIFEDIPINE

NDC 70771-1365 · HUMAN PRESCRIPTION DRUG · TABLET, EXTENDED RELEASE

Labeler / ManufacturerZydus Lifesciences Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA210184
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsNIFEDIPINE (30 mg/1)
Marketing started20180818
Package count6

External sources

Source: openFDA. Public-domain (CC0).