FDA NDC Directory · JSON-LD · Markdown

OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE

NDC 50090-7478 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerA-S Medication Solutions
Marketing categoryAbbreviated NDA (generic) · App ANDA204801
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsHYDROCHLOROTHIAZIDE (12.5 mg/1)
OLMESARTAN MEDOXOMIL (20 mg/1)
Marketing started20230602
Package count2

External sources

Source: openFDA. Public-domain (CC0).