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OLMESARTAN MEDOXOMIL

NDC 0527-2425 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic nameOlmesartan medoxomil
Labeler / ManufacturerLannett Company, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA211049
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsOLMESARTAN MEDOXOMIL (5 mg/1)
Marketing started20190305
Package count2

External sources

Source: openFDA. Public-domain (CC0).