FDA NDC Directory · JSON-LD · Markdown

Amlodipine and Olmesartan Medoxomil

NDC 69238-2673 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerAmneal Pharmaceuticals NY LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA209010
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsAMLODIPINE BESYLATE (10 mg/1)
OLMESARTAN MEDOXOMIL (20 mg/1)
Marketing started20181203
Package count1

External sources

Source: openFDA. Public-domain (CC0).