Amlodipine Besylate

NDC 70518-3592 · REMEDYREPACK INC.

Generic nameAmlodipine Besylate

Dosage formTABLET

RouteORAL

Active ingredient(s)AMLODIPINE BESYLATE

Strength5 mg/1

Pharmacologic classCalcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC], Cytochrome P450 3A Inhibitors [MoA], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS]

Marketing categoryANDA

Packages

70518-3592-0 — 30 TABLET in 1 BLISTER PACK (70518-3592-0)

70518-3592-1 — 90 TABLET in 1 BOTTLE, PLASTIC (70518-3592-1)

70518-3592-2 — 30 TABLET in 1 BOTTLE, PLASTIC (70518-3592-2)

70518-3592-3 — 90 TABLET in 1 BOTTLE, PLASTIC (70518-3592-3)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

70436-016 — olmesartan medoxomil and amlodipine besylate and hydrochlorothiazide, 70436-017 — olmesartan medoxomil and amlodipine besylate and hydrochlorothiazide, 70436-018 — olmesartan medoxomil and amlodipine besylate and hydrochlorothiazide, 70518-0297 — AMLODIPINE BESYLATE, 70518-0835 — AMLODIPINE BESYLATE, 70518-1928 — Amlodipine and Benazepril Hydrochloride, 70518-1971 — Amlodipine besylate, 70518-2566 — Amlodipine Besylate and Benazepril Hydrochloride, 70518-2632 — Amlodipine besylate, 70518-2981 — Amlodipine besylate, 70518-4165 — olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide, 70518-4382 — Amlodipine Besylate and Benazepril Hydrochloride, 70518-4386 — Amlodipine Besylate and Benazepril Hydrochloride, 70518-4388 — Amlodipine Besylate and Benazepril Hydrochloride, 70518-4464 — Amlodipine Besylate, 70518-4499 — Amlodipine Besylate and Benazepril Hydrochloride, 70518-4629 — Amlodipine besylate, 71205-122 — Amlodipine and Benazepril Hydrochloride, 71205-488 — Amlodipine besylate, 71205-506 — Amlodipine Besylate, +519 more

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