FDA NDC Directory · JSON-LD · Markdown

Olmesartan Medoxomil and Hydrochlorothiazide

NDC 50090-5450 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerA-S Medication Solutions
Marketing categoryAbbreviated NDA (generic) · App ANDA208847
Dosage form / routeTABLET · ORAL
Active ingredientsHYDROCHLOROTHIAZIDE (25 mg/1)
OLMESARTAN MEDOXOMIL (40 mg/1)
Marketing started20201001
Package count1

External sources

Source: openFDA. Public-domain (CC0).