| 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 |