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AMLODIPINE AND OLMESARTAN MEDOXOMIL

NDC 42571-238 · HUMAN PRESCRIPTION DRUG · TABLET

Generic nameAmlodipine and Olmesartan Medoxomil
Labeler / ManufacturerMicro Labs Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA207435
Dosage form / routeTABLET · ORAL
Active ingredientsAMLODIPINE BESYLATE (10 mg/1)
OLMESARTAN MEDOXOMIL (40 mg/1)
Marketing started20180101
Package count4

External sources

Source: openFDA. Public-domain (CC0).