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Felodipine

NDC 0603-3582 · HUMAN PRESCRIPTION DRUG · TABLET, EXTENDED RELEASE

Labeler / ManufacturerEndo USA, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA200815
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsFELODIPINE (5 mg/1)
Marketing started20111215
Package count2

External sources

Source: openFDA. Public-domain (CC0).