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OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE

NDC 70518-4780 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerREMEDYREPACK INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA204801
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsOLMESARTAN MEDOXOMIL (40 mg/1)
HYDROCHLOROTHIAZIDE (25 mg/1)
Marketing started20261025
Package count1

External sources

Source: openFDA. Public-domain (CC0).