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Triamterene and Hydrochlorothiazide

NDC 68001-387 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerBluePoint Laboratories
Marketing categoryAbbreviated NDA (generic) · App ANDA073449
Dosage form / routeTABLET · ORAL
Active ingredientsHYDROCHLOROTHIAZIDE (25 mg/1)
TRIAMTERENE (37.5 mg/1)
Marketing started20190618
Package count1

External sources

Source: openFDA. Public-domain (CC0).