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OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE

NDC 50228-342 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerScieGen Pharmaceuticals Inc
Marketing categoryAbbreviated NDA (generic) · App ANDA208465
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsOLMESARTAN MEDOXOMIL (20 mg/1)
HYDROCHLOROTHIAZIDE (12.5 mg/1)
Marketing started20260519
Package count3

External sources

Source: openFDA. Public-domain (CC0).