BEXXAR - 0007-3260-36 - (tositumomab)

Alphabetical Index


Drug Information of BEXXAR

Product NDC: 0007-3260
Proprietary Name: BEXXAR
Non Proprietary Name: tositumomab
Active Ingredient(s):    & nbsp;   tositumomab
Administration Route(s):
Dosage Form(s): KIT
Coding System: National Drug Codes(NDC)

Labeler Information of BEXXAR

Product NDC: 0007-3260
Labeler Name: GlaxoSmithKline LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA125011
Marketing Category: BLA
Start Marketing Date: 20090715

Package Information of BEXXAR

Package NDC: 0007-3260-36
Package Description: 1 KIT in 1 PACKAGE, COMBINATION (0007-3260-36) * 16.1 mL in 1 VIAL, SINGLE-USE * 2.5 mL in 1 VIAL, SINGLE-USE

NDC Information of BEXXAR

NDC Code 0007-3260-36
Proprietary Name BEXXAR
Package Description 1 KIT in 1 PACKAGE, COMBINATION (0007-3260-36) * 16.1 mL in 1 VIAL, SINGLE-USE * 2.5 mL in 1 VIAL, SINGLE-USE
Product NDC 0007-3260
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name tositumomab
Dosage Form Name KIT
Route Name
Start Marketing Date 20090715
Marketing Category Name BLA
Labeler Name GlaxoSmithKline LLC
Substance Name
Strength Number
Strength Unit
Pharmaceutical Classes

Complete Information of BEXXAR


General Information