Amlodipine and valsartan

NDC 65862-738 · Aurobindo Pharma Limited

Generic nameAmlodipine and valsartan

Dosage formTABLET, FILM COATED

RouteORAL

Active ingredient(s)AMLODIPINE BESYLATE, VALSARTAN

Strength5; 320 mg/1; mg/1

Pharmacologic classAngiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC], Calcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC], Cytochrome P450 3A Inhibitors [MoA], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS]

Marketing categoryANDA

Packages

65862-738-03 — 3 BLISTER PACK in 1 CARTON (65862-738-03) / 10 TABLET, FILM COATED in 1 BLISTER PACK (65862-738-10)

65862-738-30 — 30 TABLET, FILM COATED in 1 BOTTLE (65862-738-30)

65862-738-90 — 90 TABLET, FILM COATED in 1 BOTTLE (65862-738-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

65862-571 — Valsartan, 65862-572 — Valsartan, 65862-573 — Valsartan, 65862-582 — Amlodipine and Benazepril Hydrochloride, 65862-583 — Amlodipine and Benazepril Hydrochloride, 65862-584 — Amlodipine and Benazepril Hydrochloride, 65862-585 — Amlodipine and Benazepril Hydrochloride, 65862-586 — Amlodipine and Benazepril Hydrochloride, 65862-587 — Amlodipine and Benazepril Hydrochloride, 65862-737 — Amlodipine and valsartan, 65862-739 — Amlodipine and valsartan, 65862-740 — Amlodipine and valsartan, 65862-834 — Amlodipine, Valsartan and Hydrochlorothiazide, 65862-835 — Amlodipine, Valsartan and Hydrochlorothiazide, 65862-836 — Amlodipine, Valsartan and Hydrochlorothiazide, 65862-837 — Amlodipine, Valsartan and Hydrochlorothiazide, 65862-838 — Amlodipine, Valsartan and Hydrochlorothiazide, 65862-854 — Amlodipine and Olmesartan Medoxomil, 65862-855 — Amlodipine and Olmesartan Medoxomil, 65862-856 — Amlodipine and Olmesartan Medoxomil, +865 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.