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OLMESARTAN MEDOXOMIL, AMLODIPINE and HYDROCHLOROTHIAZIDE

NDC 42571-249 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic nameOlmesartan Medoxomil, Amlodipine besylate and Hydrochlorothiazide
Labeler / ManufacturerMicro Labs Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA207437
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsAMLODIPINE BESYLATE (10 mg/1)
HYDROCHLOROTHIAZIDE (25 mg/1)
OLMESARTAN MEDOXOMIL (40 mg/1)
Marketing started20260301
Package count4

External sources

Source: openFDA. Public-domain (CC0).