PERJETA - 50242-145-01 - (Pertuzumab)

Alphabetical Index


Drug Information of PERJETA

Product NDC: 50242-145
Proprietary Name: PERJETA
Non Proprietary Name: Pertuzumab
Active Ingredient(s): 30    mg/mL & nbsp;   Pertuzumab
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION, CONCENTRATE
Coding System: National Drug Codes(NDC)

Labeler Information of PERJETA

Product NDC: 50242-145
Labeler Name: Genentech, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA125409
Marketing Category: BLA
Start Marketing Date: 20120608

Package Information of PERJETA

Package NDC: 50242-145-01
Package Description: 1 VIAL, SINGLE-USE in 1 CARTON (50242-145-01) > 14 mL in 1 VIAL, SINGLE-USE

NDC Information of PERJETA

NDC Code 50242-145-01
Proprietary Name PERJETA
Package Description 1 VIAL, SINGLE-USE in 1 CARTON (50242-145-01) > 14 mL in 1 VIAL, SINGLE-USE
Product NDC 50242-145
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Pertuzumab
Dosage Form Name INJECTION, SOLUTION, CONCENTRATE
Route Name INTRAVENOUS
Start Marketing Date 20120608
Marketing Category Name BLA
Labeler Name Genentech, Inc.
Substance Name PERTUZUMAB
Strength Number 30
Strength Unit mg/mL
Pharmaceutical Classes HER2 Receptor Antagonist [EPC],HER2/Neu/cerbB2 Antagonists [MoA]

Complete Information of PERJETA


General Information