NDC 0078-1518 – Amlodipine valsartan and hydrochlorothiazide

Amlodipine Besylate 10 mg/1; Valsartan 160 mg/1; Hydrochlorothiazide 12.5 mg/1 · Tablet, Film Coated

Human Prescription Drug

Product NDC0078-1518

Product details

Brand name
Amlodipine valsartan and hydrochlorothiazide
Generic name
Amlodipine valsartan and hydrochlorothiazide
Labeler
Novartis Pharmaceuticals Corporation
Dosage form
Tablet, Film Coated
Marketing category
DRUG FOR FURTHER PROCESSING
Marketed since
April 4, 2009
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Amlodipine,valsartan and hydrochlorothiazide →

Package NDC codes (1)

Package NDCDescriptionSince
0078-1518-0160000 TABLET, FILM COATED in 1 DRUM (0078-1518-01)

Other Amlodipine,valsartan and hydrochlorothiazide products