Vectibix - 55513-954-01 - (panitumumab)

Alphabetical Index


Drug Information of Vectibix

Product NDC: 55513-954
Proprietary Name: Vectibix
Non Proprietary Name: panitumumab
Active Ingredient(s): 100    mg/5mL & nbsp;   panitumumab
Administration Route(s): INTRAVENOUS
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Vectibix

Product NDC: 55513-954
Labeler Name: Amgen Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA125147
Marketing Category: BLA
Start Marketing Date: 20061010

Package Information of Vectibix

Package NDC: 55513-954-01
Package Description: 1 VIAL, SINGLE-USE in 1 CARTON (55513-954-01) > 5 mL in 1 VIAL, SINGLE-USE

NDC Information of Vectibix

NDC Code 55513-954-01
Proprietary Name Vectibix
Package Description 1 VIAL, SINGLE-USE in 1 CARTON (55513-954-01) > 5 mL in 1 VIAL, SINGLE-USE
Product NDC 55513-954
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name panitumumab
Dosage Form Name SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20061010
Marketing Category Name BLA
Labeler Name Amgen Inc
Substance Name PANITUMUMAB
Strength Number 100
Strength Unit mg/5mL
Pharmaceutical Classes Epidermal Growth Factor Receptor Antagonist [EPC]

Complete Information of Vectibix


General Information