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amlodipine besylate

NDC 59762-2135 · Mylan Pharmaceuticals 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 categoryNDA AUTHORIZED GENERIC

Packages

59762-2135-1 — 1000 TABLET in 1 BOTTLE (59762-2135-1)

59762-2135-9 — 90 TABLET in 1 BOTTLE (59762-2135-9)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

58151-062 — amlodipine and atorvastatin, 58151-063 — amlodipine and atorvastatin, 58151-064 — amlodipine and atorvastatin, 58151-065 — amlodipine and atorvastatin, 58151-066 — amlodipine and atorvastatin, 58151-067 — amlodipine and atorvastatin, 58151-353 — amlodipine besylate, 58151-354 — amlodipine besylate, 58151-355 — amlodipine besylate, 59762-2010 — amlodipine besylate, 59762-2242 — amlodipine besylate, 60505-3478 — Amlodipine and Atorvastatin, 60505-3479 — Amlodipine and Atorvastatin, 60505-3483 — Amlodipine and Atorvastatin, 60505-3484 — Amlodipine and Atorvastatin, 60505-3488 — Amlodipine and Atorvastatin, 60505-3489 — Amlodipine and Atorvastatin, 60505-3492 — Amlodipine and Atorvastatin, 60505-3493 — Amlodipine and Atorvastatin, 60687-488 — 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.