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Amlodipine and Atorvastatin

NDC 60505-3478 · Apotex Corp.

Generic nameAmlodipine and Atorvastatin
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)AMLODIPINE BESYLATE, ATORVASTATIN CALCIUM TRIHYDRATE
Strength5; 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

60505-3478-3 — 30 TABLET, FILM COATED in 1 BOTTLE (60505-3478-3)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

58151-353 — amlodipine besylate, 58151-354 — amlodipine besylate, 58151-355 — amlodipine besylate, 59651-606 — Atorvastatin Calcium, 59651-607 — Atorvastatin Calcium, 59651-608 — Atorvastatin Calcium, 59651-609 — Atorvastatin Calcium, 59762-2010 — amlodipine besylate, 59762-2135 — amlodipine besylate, 59762-2242 — amlodipine besylate, 60505-3479 — Amlodipine and Atorvastatin, 60505-3483 — Amlodipine and Atorvastatin, 60505-3484 — Amlodipine and Atorvastatin, 60505-3488 — 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, +824 more

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