FDA NDC Directory · JSON-LD · Markdown

OLMESARTAN MEDOXOMIL

NDC 64980-601 · HUMAN PRESCRIPTION DRUG · TABLET, COATED

Generic nameolmesartan medoxomil
Labeler / ManufacturerRising Pharma Holdings, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA208659
Dosage form / routeTABLET, COATED · ORAL
Active ingredientsOLMESARTAN MEDOXOMIL (5 mg/1)
Marketing started20240330
Marketing ended20260630
Package count1

External sources

Source: openFDA. Public-domain (CC0).