Skip to main content

Amlodipine and Atorvastatin

NDC 62332-765 · Alembic Pharmaceuticals Inc.

Generic nameAmlodipine and Atorvastatin
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)AMLODIPINE BESYLATE, ATORVASTATIN CALCIUM TRIHYDRATE
Strength10; 80 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

62332-765-30 — 30 TABLET, FILM COATED in 1 BOTTLE (62332-765-30)

62332-765-90 — 90 TABLET, FILM COATED in 1 BOTTLE (62332-765-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

62332-755 — Amlodipine and Atorvastatin, 62332-756 — Amlodipine and Atorvastatin, 62332-757 — Amlodipine and Atorvastatin, 62332-758 — Amlodipine and Atorvastatin, 62332-759 — Amlodipine and Atorvastatin, 62332-760 — Amlodipine and Atorvastatin, 62332-761 — Amlodipine and Atorvastatin, 62332-762 — Amlodipine and Atorvastatin, 62332-763 — Amlodipine and Atorvastatin, 62332-764 — Amlodipine and Atorvastatin, 63187-783 — Amlodipine besylate, 63187-907 — ATORVASTATIN CALCIUM, 63187-914 — AMLODIPINE BESYLATE, 63304-829 — Atorvastatin Calcium, 63304-830 — Atorvastatin Calcium, 63629-1023 — Amlodipine besylate, 63629-1024 — Amlodipine besylate, 63629-2238 — olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide, 63629-2239 — olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide, 63629-2240 — olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide, +824 more

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