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Amlodipine Besylate

NDC 48433-155 · Safecor Health LLC

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

48433-155-20 — 100 BLISTER PACK in 1 CARTON (48433-155-20) / 1 TABLET in 1 BLISTER PACK (48433-155-01)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

46708-756 — Amlodipine and Atorvastatin, 46708-757 — Amlodipine and Atorvastatin, 46708-758 — Amlodipine and Atorvastatin, 46708-759 — Amlodipine and Atorvastatin, 46708-760 — Amlodipine and Atorvastatin, 46708-761 — Amlodipine and Atorvastatin, 46708-762 — Amlodipine and Atorvastatin, 46708-763 — Amlodipine and Atorvastatin, 46708-764 — Amlodipine and Atorvastatin, 46708-765 — Amlodipine and Atorvastatin, 48433-156 — Amlodipine Besylate, 48433-157 — Amlodipine Besylate, 49884-786 — olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide, 49884-787 — olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide, 49884-788 — olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide, 49884-789 — olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide, 49884-790 — olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide, 50090-1042 — Amlodipine and Benazepril Hydrochloride, 50090-1418 — Amlodipine and Benazepril Hydrochloride, 50090-1627 — 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.