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Amlodipine Besylate

NDC 60687-972 · HUMAN PRESCRIPTION DRUG · TABLET

Generic nameAmlodipine besylate
Labeler / ManufacturerAmerican Health Packaging
Marketing categoryAbbreviated NDA (generic) · App ANDA078925
Dosage form / routeTABLET · ORAL
Active ingredientsAMLODIPINE BESYLATE (5 mg/1)
Marketing started20261001
Package count1

External sources

Source: openFDA. Public-domain (CC0).