FDA NDC Directory · JSON-LD · Markdown

Valsartan and Hydrochlorothiazide

NDC 68180-101 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerLupin Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA078946
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsHYDROCHLOROTHIAZIDE (12.5 mg/1)
VALSARTAN (320 mg/1)
Marketing started20130321
Package count0

External sources

Source: openFDA. Public-domain (CC0).