DOFETILIDE

NDC 47335-062 · Sun Pharmaceutical Industries, Inc.

Generic nameDOFETILIDE

Dosage formCAPSULE

RouteORAL

Active ingredient(s)DOFETILIDE

Strength.25 mg/1

Pharmacologic classAntiarrhythmic [EPC]

Marketing categoryANDA

Packages

47335-062-79 — 4 BLISTER PACK in 1 CARTON (47335-062-79) / 10 CAPSULE in 1 BLISTER PACK (47335-062-66)

47335-062-86 — 60 CAPSULE in 1 BOTTLE (47335-062-86)

FDA lists these products with the same active ingredient.

0904-7522 — Dofetilide, 0904-7523 — Dofetilide, 0904-7524 — Dofetilide, 16729-490 — Dofetilide, 16729-491 — Dofetilide, 16729-492 — Dofetilide, 42794-044 — Dofetilide, 42794-045 — Dofetilide, 42794-046 — Dofetilide, 47335-061 — DOFETILIDE, 47335-063 — DOFETILIDE, 59651-118 — Dofetilide, 59651-119 — Dofetilide, 59651-120 — Dofetilide, 69452-131 — Dofetilide, 69452-132 — Dofetilide, 69452-133 — Dofetilide, 70010-024 — Dofetilide 0.125mg, 70010-025 — Dofetilide 0.25mg, 70010-026 — Dofetilide 0.5mg, +16 more

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