FDA NDC Directory · JSON-LD · Markdown

Felodipine

NDC 0603-3583 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Labeler / ManufacturerEndo USA, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA200815
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsFELODIPINE (10 mg/1)
Marketing started20111215
Package count2

External sources

Source: openFDA. Public-domain (CC0).