Amlodipine and Atorvastatin

NDC 71335-3076 · Bryant Ranch Prepack

Generic nameAmlodipine and Atorvastatin

Dosage formTABLET, FILM COATED

RouteORAL

Active ingredient(s)AMLODIPINE BESYLATE, ATORVASTATIN CALCIUM TRIHYDRATE

Strength10; 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

71335-3076-1 — 30 TABLET, FILM COATED in 1 BOTTLE (71335-3076-1)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

71335-2493 — ATORVASTATIN CALCIUM, 71335-2507 — Amlodipine Besylate, 71335-2582 — atorvastatin calcium, film coated, 71335-2591 — atorvastatin calcium, film coated, 71335-2634 — Amlodipine Besylate and Benazepril Hydrochloride, 71335-2799 — Atorvastatin calcium, 71335-2924 — Amlodipine and Atorvastatin, 71335-2977 — Atorvastatin calcium, 71335-3055 — Amlodipine Besylate and Benazepril Hydrochloride, 71335-3067 — Amlodipine Besylate and Benazepril Hydrochloride, 71335-3095 — Amlodipine Besylate and Benazepril Hydrochloride, 71335-3125 — Amlodipine Besylate and Benazepril Hydrochloride, 71335-3126 — Amlodipine besylate, 71335-3144 — Atorvastatin Calcium, 71335-9711 — Atorvastatin calcium, 71335-9723 — Atorvastatin Calcium, 71610-022 — ATORVASTATIN CALCIUM, 71610-036 — ATORVASTATIN CALCIUM, 71610-163 — ATORVASTATIN CALCIUM, 71610-469 — 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.