FDA NDC Directory · JSON-LD · Markdown

HYDROCHLOROTHIAZIDE

NDC 23155-009 · HUMAN PRESCRIPTION DRUG · TABLET

Generic namehydrochlorothiazide
Labeler / ManufacturerHeritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA085182
Dosage form / routeTABLET · ORAL
Active ingredientsHYDROCHLOROTHIAZIDE (50 mg/1)
Marketing started20150115
Package count4

External sources

Source: openFDA. Public-domain (CC0).