FDA NDC Directory · JSON-LD · Markdown

OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE

NDC 72603-292 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerNorthStar RxLLC
Marketing categoryAbbreviated NDA (generic) · App ANDA204801
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsHYDROCHLOROTHIAZIDE (25 mg/1)
OLMESARTAN MEDOXOMIL (40 mg/1)
Marketing started20240408
Package count2

External sources

Source: openFDA. Public-domain (CC0).