AMLODIPINE BESYLATE

NDC 70518-0297 · REMEDYREPACK INC.

Generic nameAMLODIPINE BESYLATE

Dosage formTABLET

RouteORAL

Active ingredient(s)AMLODIPINE BESYLATE

Strength10 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

70518-0297-0 — 30 TABLET in 1 BLISTER PACK (70518-0297-0)

70518-0297-1 — 90 TABLET in 1 BOTTLE, PLASTIC (70518-0297-1)

70518-0297-4 — 50 POUCH in 1 BOX (70518-0297-4) / 1 TABLET in 1 POUCH (70518-0297-5)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

69238-2686 — Amlodipine Besylate and Benazepril Hydrochloride, 69238-2687 — Amlodipine Besylate and Benazepril Hydrochloride, 69584-021 — AMLODIPINE BESYLATE, 69584-022 — AMLODIPINE BESYLATE, 69584-023 — AMLODIPINE BESYLATE, 70436-014 — olmesartan medoxomil and amlodipine besylate and hydrochlorothiazide, 70436-015 — olmesartan medoxomil and amlodipine besylate and hydrochlorothiazide, 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, 70518-0835 — 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, 70518-3592 — Amlodipine Besylate, 70518-4165 — olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide, 70518-4382 — Amlodipine Besylate and Benazepril Hydrochloride, 70518-4386 — Amlodipine Besylate and Benazepril Hydrochloride, +519 more

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