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Amlodipine Besylate

NDC 0615-8429 · HUMAN PRESCRIPTION DRUG · TABLET

Generic nameAmlodipine besylate
Labeler / ManufacturerNCS HealthCare of KY, LLC dba Vangard Labs
Marketing categoryAbbreviated NDA (generic) · App ANDA078925
Dosage form / routeTABLET · ORAL
Active ingredientsAMLODIPINE BESYLATE (2.5 mg/1)
Marketing started20101020
Marketing ended20260930
Package count2

External sources

Source: openFDA. Public-domain (CC0).