FDA NDC Directory · JSON-LD · Markdown

olmesartan medoxomil

NDC 50090-3471 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerA-S Medication Solutions
Marketing categoryAbbreviated NDA (generic) · App ANDA207662
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsOLMESARTAN MEDOXOMIL (20 mg/1)
Marketing started20170427
Package count2

External sources

Source: openFDA. Public-domain (CC0).