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amlodipine,valsartan and hydrochlorothiazide

NDC 33342-285 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerMacleods Pharmaceuticals Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA207299
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsAMLODIPINE BESYLATE (5 mg/1)
HYDROCHLOROTHIAZIDE (25 mg/1)
VALSARTAN (160 mg/1)
Marketing started20250106
Package count3

External sources

Source: openFDA. Public-domain (CC0).