Amlodipine Besylate

NDC 68382-122 · Zydus Pharmaceuticals USA 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

68382-122-01 — 100 TABLET in 1 BOTTLE (68382-122-01)

68382-122-05 — 500 TABLET in 1 BOTTLE (68382-122-05)

68382-122-16 — 90 TABLET in 1 BOTTLE (68382-122-16)

68382-122-77 — 10 BLISTER PACK in 1 CARTON (68382-122-77) / 10 TABLET in 1 BLISTER PACK

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68180-764 — Amlodipine and Valsartan, 68180-765 — Amlodipine and Valsartan, 68180-766 — Amlodipine and Valsartan, 68180-767 — Amlodipine and Valsartan, 68180-771 — Amlodipine, Valsartan and Hydrochlorothiazide, 68180-772 — Amlodipine, Valsartan and Hydrochlorothiazide, 68180-773 — Amlodipine, Valsartan and Hydrochlorothiazide, 68180-774 — Amlodipine, Valsartan and Hydrochlorothiazide, 68180-775 — Amlodipine, Valsartan and Hydrochlorothiazide, 68382-121 — Amlodipine Besylate, 68382-123 — Amlodipine Besylate, 68462-566 — Amlodipine and Olmesartan Medoxomil, 68462-567 — Amlodipine and Olmesartan Medoxomil, 68462-568 — Amlodipine and Olmesartan Medoxomil, 68462-569 — Amlodipine and Olmesartan Medoxomil, 68645-515 — Amlodipine Besylate, 68645-516 — Amlodipine Besylate, 68645-580 — AMLODIPINE BESYLATE, 68788-4082 — Amlodipine Besylate, 68788-4085 — 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.