FDA NDC Directory · JSON-LD · Markdown

OLMESARTAN MEDOXOMIL

NDC 72303-0849 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic nameOlmesartan medoxomil
Labeler / ManufacturerHEC Pharm USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA211049
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsOLMESARTAN MEDOXOMIL (20 mg/1)
Marketing started20260410
Package count2

External sources

Source: openFDA. Public-domain (CC0).