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FELODIPINE

NDC 23155-048 · HUMAN PRESCRIPTION DRUG · TABLET, EXTENDED RELEASE

Labeler / ManufacturerHeritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA201964
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsFELODIPINE (2.5 mg/1)
Marketing started20131108
Package count2

External sources

Source: openFDA. Public-domain (CC0).