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Felodipine

NDC 69117-0029 · HUMAN PRESCRIPTION DRUG · TABLET, EXTENDED RELEASE

Generic nameFelodipine Extended-release Tablets
Labeler / ManufacturerYiling Pharmaceutical Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA210847
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsFELODIPINE (5 mg/1)
Marketing started20190801
Package count2

External sources

Source: openFDA. Public-domain (CC0).