Amlodipine and Valsartan

NDC 46708-460 · Alembic Pharmaceuticals 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

46708-460-10 — 100 TABLET, FILM COATED in 1 CARTON (46708-460-10)

46708-460-30 — 30 TABLET, FILM COATED in 1 BOTTLE (46708-460-30)

46708-460-31 — 100 TABLET, FILM COATED in 1 BOTTLE (46708-460-31)

46708-460-71 — 500 TABLET, FILM COATED in 1 BOTTLE (46708-460-71)

46708-460-90 — 90 TABLET, FILM COATED in 1 BOTTLE (46708-460-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

46708-213 — Amlodipine besylate and Olmesartran medoxomil, 46708-214 — Amlodipine besylate and Olmesartran medoxomil, 46708-215 — Amlodipine besylate and Olmesartran medoxomil, 46708-453 — Valsartan and Hydrochlorothiazide, 46708-454 — Valsartan and Hydrochlorothiazide, 46708-455 — Valsartan and Hydrochlorothiazide, 46708-456 — Valsartan and Hydrochlorothiazide, 46708-457 — Valsartan and Hydrochlorothiazide, 46708-458 — Amlodipine and Valsartan, 46708-459 — Amlodipine and Valsartan, 46708-461 — Amlodipine and Valsartan, 46708-556 — sacubitril and valsartan, 46708-557 — sacubitril and valsartan, 46708-558 — sacubitril and valsartan, 46708-755 — Amlodipine and Atorvastatin, 46708-756 — Amlodipine and Atorvastatin, 46708-757 — Amlodipine and Atorvastatin, 46708-758 — Amlodipine and Atorvastatin, 46708-759 — Amlodipine and Atorvastatin, 46708-760 — Amlodipine and Atorvastatin, +865 more

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