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IRBESARTAN AND HYDROCHLOROTHIAZIDE

NDC 42658-142 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic nameirbesartan and hydrochlorothiazide
Labeler / ManufacturerHisun Pharmaceuticals USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA207896
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsHYDROCHLOROTHIAZIDE (12.5 mg/1)
IRBESARTAN (300 mg/1)
Marketing started20250101
Package count3

External sources

Source: openFDA. Public-domain (CC0).