NDC 47335-062 – Dofetilide

Dofetilide .25 mg/1 · Capsule · Oral

Human Prescription Drug 1 recall

Product NDC47335-062

Product details

Brand name
Dofetilide
Generic name
Dofetilide
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA210466
Marketed since
October 11, 2018
Listing expires
December 31, 2026
Pharmacologic class
Antiarrhythmic

Active ingredients

Uses, dosage, side effects and warnings for Dofetilide →

Package NDC codes (2)

Package NDCDescriptionSince
47335-062-794 BLISTER PACK in 1 CARTON (47335-062-79) / 10 CAPSULE in 1 BLISTER PACK (47335-062-66)Oct 11, 2018
47335-062-8660 CAPSULE in 1 BOTTLE (47335-062-86)Oct 11, 2018

Recalls mentioning this NDC

Other Dofetilide products