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Amlodipine Besylate

NDC 65862-101 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAurobindo Pharma Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA078021
Dosage form / routeTABLET · ORAL
Active ingredientsAMLODIPINE BESYLATE (2.5 mg/1)
Marketing started20070717
Package count4

External sources

Source: openFDA. Public-domain (CC0).