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Felodipine

NDC 57237-108 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Labeler / ManufacturerRising Pharma Holdings, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA203417
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsFELODIPINE (2.5 mg/1)
Marketing started20130117
Package count1

External sources

Source: openFDA. Public-domain (CC0).