Amlodipine and Atorvastatin

NDC 60505-3488 · Apotex Corp.

Generic nameAmlodipine and Atorvastatin

Dosage formTABLET, FILM COATED

RouteORAL

Active ingredient(s)AMLODIPINE BESYLATE, ATORVASTATIN CALCIUM TRIHYDRATE

Strength5; 40 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

60505-3488-3 — 30 TABLET, FILM COATED in 1 BOTTLE (60505-3488-3)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

59651-607 — Atorvastatin Calcium, 59651-608 — Atorvastatin Calcium, 59651-609 — Atorvastatin Calcium, 59762-2010 — amlodipine besylate, 59762-2135 — amlodipine besylate, 59762-2242 — amlodipine besylate, 60505-3478 — Amlodipine and Atorvastatin, 60505-3479 — Amlodipine and Atorvastatin, 60505-3483 — Amlodipine and Atorvastatin, 60505-3484 — Amlodipine and Atorvastatin, 60505-3489 — Amlodipine and Atorvastatin, 60505-3492 — Amlodipine and Atorvastatin, 60505-3493 — Amlodipine and Atorvastatin, 60687-488 — Amlodipine besylate, 60687-496 — Amlodipine besylate, 60760-445 — Amlodipine Besylate, 60760-666 — Atorvastatin calcium, 60760-726 — Atorvastatin calcium, 60760-734 — atorvastatin calcium, 60760-882 — 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.

Read from: FDA National Drug Code Directory, product.txt and package.txt (accessdata.fda.gov/cder/ndctext.zip) — Snapshot retrieved 2026-08-24, loaded 2026-08-24; CMS Medicare Part B Drug Average Sales Price (ASP) Pricing Files (cms.gov/medicare/payment/part-b-drugs/asp-pricing-files) -- the NDC-HCPCS crosswalk and Part B payment limit files — 2026 Q3 (July 2026 release). All data sources · How to read the labels