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TNKase
TNKase - 50242-120-01 - (tenecteplase)
Drug Information of TNKase
| Product NDC: | 50242-120 |
| Proprietary Name: | TNKase |
| Non Proprietary Name: | tenecteplase |
| Active Ingredient(s): | & nbsp; tenecteplase |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of TNKase
| Product NDC: | 50242-120 |
| Labeler Name: | Genentech, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | BLA103909 |
| Marketing Category: | BLA |
| Start Marketing Date: | 20000602 |
Package Information of TNKase
| Package NDC: | 50242-120-01 |
| Package Description: | 1 KIT in 1 CARTON (50242-120-01) * 50 mg in 1 VIAL, SINGLE-USE * 10 mL in 1 VIAL, SINGLE-USE |
NDC Information of TNKase
| NDC Code | 50242-120-01 |
| Proprietary Name | TNKase |
| Package Description | 1 KIT in 1 CARTON (50242-120-01) * 50 mg in 1 VIAL, SINGLE-USE * 10 mL in 1 VIAL, SINGLE-USE |
| Product NDC | 50242-120 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | tenecteplase |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20000602 |
| Marketing Category Name | BLA |
| Labeler Name | Genentech, Inc. |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
