Caduet

NDC 58151-067 · Viatris Specialty LLC

Generic nameamlodipine and atorvastatin

Dosage formTABLET, FILM COATED

RouteORAL

Active ingredient(s)AMLODIPINE BESYLATE, ATORVASTATIN CALCIUM TRIHYDRATE

Strength5; 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 categoryNDA

Packages

58151-067-93 — 30 TABLET, FILM COATED in 1 BOTTLE (58151-067-93)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

57237-143 — Amlodipine and Benazepril Hydrochloride, 57237-144 — Amlodipine and Benazepril Hydrochloride, 57237-145 — Amlodipine and Benazepril Hydrochloride, 57237-146 — Amlodipine and Benazepril Hydrochloride, 57237-147 — Amlodipine and Benazepril Hydrochloride, 58151-062 — amlodipine and atorvastatin, 58151-063 — amlodipine and atorvastatin, 58151-064 — amlodipine and atorvastatin, 58151-065 — amlodipine and atorvastatin, 58151-066 — amlodipine and atorvastatin, 58151-155 — atorvastatin calcium, 58151-156 — atorvastatin calcium, 58151-157 — atorvastatin calcium, 58151-158 — atorvastatin calcium, 58151-353 — amlodipine besylate, 58151-354 — amlodipine besylate, 58151-355 — amlodipine besylate, 59651-606 — Atorvastatin Calcium, 59651-607 — Atorvastatin Calcium, 59651-608 — 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.