FDA NDC Directory · JSON-LD · Markdown

olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide

NDC 70518-4165 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerREMEDYREPACK INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA206137
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsAMLODIPINE BESYLATE (5 mg/1)
HYDROCHLOROTHIAZIDE (25 mg/1)
OLMESARTAN MEDOXOMIL (40 mg/1)
Marketing started20240822
Package count1

External sources

Source: openFDA. Public-domain (CC0).