FDA NDC Directory · JSON-LD · Markdown

Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide

NDC 0093-5006 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerTeva Pharmaceuticals USA, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA202491
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsAMLODIPINE BESYLATE (5 mg/1)
HYDROCHLOROTHIAZIDE (12.5 mg/1)
OLMESARTAN MEDOXOMIL (40 mg/1)
Marketing started20161114
Package count1

External sources

Source: openFDA. Public-domain (CC0).