FDA NDC Directory · JSON-LD · Markdown

Olmesartan Medoxomil and Hydrochlorothiazide

NDC 50090-3561 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerA-S Medication Solutions
Marketing categoryAbbreviated NDA (generic) · App ANDA205391
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsHYDROCHLOROTHIAZIDE (12.5 mg/1)
OLMESARTAN MEDOXOMIL (40 mg/1)
Marketing started20170424
Package count1

External sources

Source: openFDA. Public-domain (CC0).