FDA NDC Directory · JSON-LD · Markdown

HYDROCHLOROTHIAZIDE

NDC 69315-130 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerLeading Pharma, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA040702
Dosage form / routeTABLET · ORAL
Active ingredientsHYDROCHLOROTHIAZIDE (50 mg/1)
Marketing started20160401
Package count2

External sources

Source: openFDA. Public-domain (CC0).