Tikosyn - 0069-5800-43 - (dofetilide)

Alphabetical Index


Drug Information of Tikosyn

Product NDC: 0069-5800
Proprietary Name: Tikosyn
Non Proprietary Name: dofetilide
Active Ingredient(s): .125    mg/1 & nbsp;   dofetilide
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Tikosyn

Product NDC: 0069-5800
Labeler Name: Pfizer Laboratories Div Pfizer Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020931
Marketing Category: NDA
Start Marketing Date: 19991001

Package Information of Tikosyn

Package NDC: 0069-5800-43
Package Description: 40 CAPSULE in 1 BOTTLE, UNIT-DOSE (0069-5800-43)

NDC Information of Tikosyn

NDC Code 0069-5800-43
Proprietary Name Tikosyn
Package Description 40 CAPSULE in 1 BOTTLE, UNIT-DOSE (0069-5800-43)
Product NDC 0069-5800
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name dofetilide
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 19991001
Marketing Category Name NDA
Labeler Name Pfizer Laboratories Div Pfizer Inc
Substance Name DOFETILIDE
Strength Number .125
Strength Unit mg/1
Pharmaceutical Classes Antiarrhythmic [EPC]

Complete Information of Tikosyn


General Information