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Amlodipine Besylate

NDC 71335-0890 · Bryant Ranch Prepack

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

71335-0890-1 30 TABLET in 1 BOTTLE (71335-0890-1)

71335-0890-2 90 TABLET in 1 BOTTLE (71335-0890-2)

71335-0890-3 120 TABLET in 1 BOTTLE (71335-0890-3)

71335-0890-4 60 TABLET in 1 BOTTLE (71335-0890-4)

71335-0890-5 500 TABLET in 1 BOTTLE (71335-0890-5)

71335-0890-6 10 TABLET in 1 BOTTLE (71335-0890-6)

71335-0890-7 100 TABLET in 1 BOTTLE (71335-0890-7)

71335-0890-8 180 TABLET in 1 BOTTLE (71335-0890-8)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

70518-4629 — Amlodipine besylate, 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, 71335-0945 — Amlodipine Besylate, 71335-0953 — Amlodipine and Benazepril Hydrochloride, 71335-1278 — Amlodipine besylate, 71335-1865 — Amlodipine Besylate, 71335-1887 — AMLODIPINE BESYLATE, 71335-1946 — Amlodipine Besylate and Benazepril Hydrochloride, 71335-2359 — Amlodipine Besylate, 71335-2507 — Amlodipine Besylate, 71335-2634 — Amlodipine Besylate and Benazepril Hydrochloride, 71335-2924 — Amlodipine and Atorvastatin, +519 more

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