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Amlodipine Besylate

NDC 70518-4629 · REMEDYREPACK INC.

Generic nameAmlodipine besylate
Dosage formTABLET
RouteORAL
Active ingredient(s)AMLODIPINE BESYLATE
Strength2.5 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

70518-4629-0 — 50 POUCH in 1 BOX (70518-4629-0) / 1 TABLET in 1 POUCH (70518-4629-1)

70518-4629-2 — 30 TABLET in 1 BLISTER PACK (70518-4629-2)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

70518-2566 — Amlodipine Besylate and Benazepril Hydrochloride, 70518-2632 — Amlodipine besylate, 70518-2981 — Amlodipine besylate, 70518-3592 — 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, 71205-122 — Amlodipine and Benazepril Hydrochloride, 71205-488 — Amlodipine besylate, 71205-506 — Amlodipine Besylate, 71205-596 — Amlodipine besylate, 71205-599 — Amlodipine Besylate, 71335-0218 — AMLODIPINE BESYLATE, 71335-0473 — AMLODIPINE BESYLATE, 71335-0833 — Amlodipine besylate, 71335-0843 — Amlodipine besylate, 71335-0890 — 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.