TYSABRI - 59075-730-15 - (natalizumab)

Alphabetical Index


Drug Information of TYSABRI

Product NDC: 59075-730
Proprietary Name: TYSABRI
Non Proprietary Name: natalizumab
Active Ingredient(s): 300    mg/15mL & nbsp;   natalizumab
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of TYSABRI

Product NDC: 59075-730
Labeler Name: Elan Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA125104
Marketing Category: BLA
Start Marketing Date: 20041123

Package Information of TYSABRI

Package NDC: 59075-730-15
Package Description: 1 VIAL, SINGLE-USE in 1 CARTON (59075-730-15) > 1 mL in 1 VIAL, SINGLE-USE

NDC Information of TYSABRI

NDC Code 59075-730-15
Proprietary Name TYSABRI
Package Description 1 VIAL, SINGLE-USE in 1 CARTON (59075-730-15) > 1 mL in 1 VIAL, SINGLE-USE
Product NDC 59075-730
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name natalizumab
Dosage Form Name INJECTION
Route Name INTRAVENOUS
Start Marketing Date 20041123
Marketing Category Name BLA
Labeler Name Elan Pharmaceuticals, Inc.
Substance Name NATALIZUMAB
Strength Number 300
Strength Unit mg/15mL
Pharmaceutical Classes Integrin Receptor Antagonist [EPC],Integrin Receptor Antagonists [MoA]

Complete Information of TYSABRI


General Information