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Amlodipine Besylate

NDC 69097-837 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerCipla USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA077955
Dosage form / routeTABLET · ORAL
Active ingredientsAMLODIPINE BESYLATE (5 mg/1)
Marketing started20160701
Package count2

External sources

Source: openFDA. Public-domain (CC0).