Amlodipine and Atorvastatin

NDC 46708-755 · Alembic Pharmaceuticals Limited

Generic nameAmlodipine and Atorvastatin

Dosage formTABLET, FILM COATED

RouteORAL

Active ingredient(s)AMLODIPINE BESYLATE, ATORVASTATIN CALCIUM TRIHYDRATE

Strength2.5; 10 mg/1; mg/1

Pharmacologic classCalcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC], Cytochrome P450 3A Inhibitors [MoA], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS], HMG-CoA Reductase Inhibitor [EPC], Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]

Marketing categoryANDA

Packages

46708-755-30 — 30 TABLET, FILM COATED in 1 BOTTLE (46708-755-30)

46708-755-90 — 90 TABLET, FILM COATED in 1 BOTTLE (46708-755-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

46708-186 — Telmisartan and Amlodipine, 46708-187 — Telmisartan and Amlodipine, 46708-212 — Amlodipine besylate and Olmesartran medoxomil, 46708-213 — Amlodipine besylate and Olmesartran medoxomil, 46708-214 — Amlodipine besylate and Olmesartran medoxomil, 46708-215 — Amlodipine besylate and Olmesartran medoxomil, 46708-458 — Amlodipine and Valsartan, 46708-459 — Amlodipine and Valsartan, 46708-460 — Amlodipine and Valsartan, 46708-461 — Amlodipine and Valsartan, 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, 46708-761 — Amlodipine and Atorvastatin, 46708-762 — Amlodipine and Atorvastatin, 46708-763 — Amlodipine and Atorvastatin, 46708-764 — Amlodipine and Atorvastatin, 46708-765 — Amlodipine and Atorvastatin, +824 more

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