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triamterene and hydrochlorothiazide

NDC 70771-1362 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerZydus Lifesciences Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA208360
Dosage form / routeTABLET · ORAL
Active ingredientsHYDROCHLOROTHIAZIDE (50 mg/1)
TRIAMTERENE (75 mg/1)
Marketing started20180904
Package count4

External sources

Source: openFDA. Public-domain (CC0).