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OLMESARTAN MEDOXOMIL AND HYDROCHLOROTHIAZIDE

NDC 70518-4577 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerREMEDYREPACK INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA207037
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsHYDROCHLOROTHIAZIDE (25 mg/1)
OLMESARTAN MEDOXOMIL (40 mg/1)
Marketing started20260227
Package count1

External sources

Source: openFDA. Public-domain (CC0).