FDA NDC Directory · JSON-LD · Markdown

Hydrochlorothiazide

NDC 65862-134 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAurobindo Pharma Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA040780
Dosage form / routeTABLET · ORAL
Active ingredientsHYDROCHLOROTHIAZIDE (50 mg/1)
Marketing started20070720
Package count2

External sources

Source: openFDA. Public-domain (CC0).