FDA NDC Directory · JSON-LD · Markdown

Olmesartan medoxomil Amlodipine and Hydrochlorothiazide

NDC 33342-243 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerMacleods Pharmaceuticals Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA207088
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsAMLODIPINE BESYLATE (5 mg/1)
HYDROCHLOROTHIAZIDE (12.5 mg/1)
OLMESARTAN MEDOXOMIL (20 mg/1)
Marketing started20250718
Package count2

External sources

Source: openFDA. Public-domain (CC0).