NDC 65862-834 – Amlodipine, Valsartan and Hydrochlorothiazide

Amlodipine Besylate 5 mg/1; Valsartan 160 mg/1; Hydrochlorothiazide 12.5 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC65862-834

Product details

Brand name
Amlodipine, Valsartan and Hydrochlorothiazide
Generic name
Amlodipine, Valsartan and Hydrochlorothiazide
Labeler
Aurobindo Pharma Limited
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA206180
Marketed since
December 19, 2017
Listing expires
December 31, 2026
Pharmacologic class
Angiotensin 2 Receptor Blocker; Calcium Channel Blocker; Dihydropyridine Calcium Channel Blocker; Thiazide Diuretic

Active ingredients

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

Package NDC codes (3)

Package NDCDescriptionSince
65862-834-05500 TABLET, FILM COATED in 1 BOTTLE (65862-834-05)Dec 19, 2017
65862-834-3030 TABLET, FILM COATED in 1 BOTTLE (65862-834-30)Dec 19, 2017
65862-834-9090 TABLET, FILM COATED in 1 BOTTLE (65862-834-90)Dec 19, 2017

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