AMLODIPINE BESYLATE

NDC 69584-022 · Oxford Pharmaceuticals, LLC

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

69584-022-09 — 90 TABLET in 1 BOTTLE (69584-022-09)

69584-022-50 — 500 TABLET in 1 BOTTLE (69584-022-50)

69584-022-90 — 1000 TABLET in 1 BOTTLE (69584-022-90)

69584-022-95 — 5000 TABLET in 1 BOTTLE (69584-022-95)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

69097-838 — Amlodipine Besylate, 69238-2673 — Amlodipine and Olmesartan Medoxomil, 69238-2674 — Amlodipine and Olmesartan Medoxomil, 69238-2675 — Amlodipine and Olmesartan Medoxomil, 69238-2676 — Amlodipine and Olmesartan Medoxomil, 69238-2684 — Amlodipine Besylate and Benazepril Hydrochloride, 69238-2685 — Amlodipine Besylate and Benazepril Hydrochloride, 69238-2686 — Amlodipine Besylate and Benazepril Hydrochloride, 69238-2687 — Amlodipine Besylate and Benazepril Hydrochloride, 69584-021 — 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, 70518-0297 — AMLODIPINE BESYLATE, 70518-0835 — AMLODIPINE BESYLATE, 70518-1928 — Amlodipine and Benazepril Hydrochloride, 70518-1971 — 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.