FDA NDC Directory · JSON-LD · Markdown

Olmesartan Medoxomil and Hydrochlorothiazide

NDC 71335-2180 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerBryant Ranch Prepack
Marketing categoryAbbreviated NDA (generic) · App ANDA208847
Dosage form / routeTABLET · ORAL
Active ingredientsHYDROCHLOROTHIAZIDE (12.5 mg/1)
OLMESARTAN MEDOXOMIL (40 mg/1)
Marketing started20201001
Package count3

External sources

Source: openFDA. Public-domain (CC0).