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] |