FDA NDC Directory · JSON-LD · Markdown

Hydrochlorothiazide

NDC 50228-111 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerScieGen Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA203018
Dosage form / routeTABLET · ORAL
Active ingredientsHYDROCHLOROTHIAZIDE (25 mg/1)
Marketing started20140723
Package count2

External sources

Source: openFDA. Public-domain (CC0).