FDA NDC Directory · JSON-LD · Markdown

Olmesartan Medoxomil and Hydrochlorothiazide

NDC 70518-2269 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerREMEDYREPACK INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA204233
Dosage form / routeTABLET · ORAL
Active ingredientsHYDROCHLOROTHIAZIDE (12.5 mg/1)
OLMESARTAN MEDOXOMIL (40 mg/1)
Marketing started20190816
Package count1

External sources

Source: openFDA. Public-domain (CC0).