| Product NDC: | 50242-044 | 
| Proprietary Name: | Activase | 
| Non Proprietary Name: | Alteplase | 
| Active Ingredient(s): | & nbsp; Alteplase | 
| Administration Route(s): | |
| Dosage Form(s): | KIT | 
| Coding System: | National Drug Codes(NDC) | 
| Product NDC: | 50242-044 | 
| Labeler Name: | Genentech, Inc. | 
| Product Type: | HUMAN PRESCRIPTION DRUG | 
| FDA Application Number: | BLA103172 | 
| Marketing Category: | BLA | 
| Start Marketing Date: | 19871113 | 
| Package NDC: | 50242-044-13 | 
| Package Description: | 1 KIT in 1 CARTON (50242-044-13) * 50 mL in 1 VIAL, SINGLE-USE * 50 mL in 1 VIAL, SINGLE-USE | 
| NDC Code | 50242-044-13 | 
| Proprietary Name | Activase | 
| Package Description | 1 KIT in 1 CARTON (50242-044-13) * 50 mL in 1 VIAL, SINGLE-USE * 50 mL in 1 VIAL, SINGLE-USE | 
| Product NDC | 50242-044 | 
| Product Type Name | HUMAN PRESCRIPTION DRUG | 
| Non Proprietary Name | Alteplase | 
| Dosage Form Name | KIT | 
| Route Name | |
| Start Marketing Date | 19871113 | 
| Marketing Category Name | BLA | 
| Labeler Name | Genentech, Inc. | 
| Substance Name | |
| Strength Number | |
| Strength Unit | |
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