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OLMESARTAN MEDOXOMIL and HYDROCHOLOROTHIAZIDE

NDC 42571-204 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic nameOlmesartan medoxomil and hydrocholorothiazide
Labeler / ManufacturerMicro Labs Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA206371
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsOLMESARTAN MEDOXOMIL (20 mg/1)
HYDROCHLOROTHIAZIDE (12.5 mg/1)
Marketing started20261015
Package count4

External sources

Source: openFDA. Public-domain (CC0).