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Amlodipine Besylate

NDC 68180-721 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerLupin Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA078043
Dosage form / routeTABLET · ORAL
Active ingredientsAMLODIPINE BESYLATE (10 mg/1)
Marketing started20180815
Package count2

External sources

Source: openFDA. Public-domain (CC0).