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Amlodipine Besylate

NDC 0480-0083 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerTeva Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA076846
Dosage form / routeTABLET · ORAL
Active ingredientsAMLODIPINE BESYLATE (2.5 mg/1)
Marketing started20221001
Package count1

External sources

Source: openFDA. Public-domain (CC0).