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AMLODIPINE and OLMESARTAN medoxomil

NDC 33342-191 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerMacleods Pharmaceuticals Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA206884
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsAMLODIPINE BESYLATE (5 mg/1)
OLMESARTAN MEDOXOMIL (40 mg/1)
Marketing started20161027
Package count4

External sources

Source: openFDA. Public-domain (CC0).