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HYDROCHLOROTHIAZIDE

NDC 70518-3633 · HUMAN PRESCRIPTION DRUG · TABLET

Generic namehydrochlorothiazide
Labeler / ManufacturerREMEDYREPACK INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA085182
Dosage form / routeTABLET · ORAL
Active ingredientsHYDROCHLOROTHIAZIDE (25 mg/1)
Marketing started20230206
Marketing ended20260630
Package count3

External sources

Source: openFDA. Public-domain (CC0).