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