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Olmesartan Medoxomil

NDC 68462-438 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerGlenmark Pharmaceuticals Inc., USA
Marketing categoryAbbreviated NDA (generic) · App ANDA203281
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsOLMESARTAN MEDOXOMIL (40 mg/1)
Marketing started20170525
Package count4

External sources

Source: openFDA. Public-domain (CC0).