FDA NDC Directory · JSON-LD · Markdown

olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide

NDC 49884-787 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerPar Health USA, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA206137
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsAMLODIPINE BESYLATE (5 mg/1)
HYDROCHLOROTHIAZIDE (12.5 mg/1)
OLMESARTAN MEDOXOMIL (40 mg/1)
Marketing started20161026
Package count2

External sources

Source: openFDA. Public-domain (CC0).