NDC 0069-5800 – Tikosyn

Dofetilide .125 mg/1 · Capsule · Oral

Human Prescription Drug 1 recall

Product NDC0069-5800

Product details

Brand name
Tikosyn
Generic name
dofetilide
Labeler
Pfizer Laboratories Div Pfizer Inc
Dosage form
Capsule
Route
Oral
Marketing category
NDA · NDA020931
Marketed since
October 1, 1999
Listing expires
December 31, 2027
Pharmacologic class
Antiarrhythmic

Active ingredients

Uses, dosage, side effects and warnings for Tikosyn →

Package NDC codes (2)

Package NDCDescriptionSince
0069-5800-6060 CAPSULE in 1 BOTTLE (0069-5800-60)Oct 1, 1999
0069-5800-6114 CAPSULE in 1 BOTTLE (0069-5800-61)Oct 1, 1999

Recalls mentioning this NDC

Other Tikosyn products