Amlodipine and Atorvastatin

NDC 46708-759 · Alembic Pharmaceuticals Limited

Generic nameAmlodipine and Atorvastatin

Dosage formTABLET, FILM COATED

RouteORAL

Active ingredient(s)AMLODIPINE BESYLATE, ATORVASTATIN CALCIUM TRIHYDRATE

Strength5; 20 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

46708-759-30 — 30 TABLET, FILM COATED in 1 BOTTLE (46708-759-30)

46708-759-90 — 90 TABLET, FILM COATED in 1 BOTTLE (46708-759-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 46708-755 — Amlodipine and Atorvastatin, 46708-756 — Amlodipine and Atorvastatin, 46708-757 — Amlodipine and Atorvastatin, 46708-758 — 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, 48433-007 — atorvastatin calcium, 48433-008 — atorvastatin calcium, 48433-009 — atorvastatin calcium, 48433-010 — atorvastatin calcium, +824 more

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