FDA NDC Directory · JSON-LD · Markdown

Hydrochlorothiazide

NDC 72789-303 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerPD-Rx Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA040907
Dosage form / routeTABLET · ORAL
Active ingredientsHYDROCHLOROTHIAZIDE (50 mg/1)
Marketing started20080815
Package count1

External sources

Source: openFDA. Public-domain (CC0).