Product NDC: | 50242-041 |
Proprietary Name: | Cathflo Activase |
Non Proprietary Name: | Alteplase |
Active Ingredient(s): | 2.2 mg/2mL & nbsp; Alteplase |
Administration Route(s): | INTRAVENOUS |
Dosage Form(s): | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 50242-041 |
Labeler Name: | Genentech, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | BLA103172 |
Marketing Category: | BLA |
Start Marketing Date: | 20010904 |
Package NDC: | 50242-041-64 |
Package Description: | 1 VIAL in 1 CARTON (50242-041-64) > 2 mL in 1 VIAL |
NDC Code | 50242-041-64 |
Proprietary Name | Cathflo Activase |
Package Description | 1 VIAL in 1 CARTON (50242-041-64) > 2 mL in 1 VIAL |
Product NDC | 50242-041 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Alteplase |
Dosage Form Name | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 20010904 |
Marketing Category Name | BLA |
Labeler Name | Genentech, Inc. |
Substance Name | ALTEPLASE |
Strength Number | 2.2 |
Strength Unit | mg/2mL |
Pharmaceutical Classes |