Product NDC: | 25208-002 |
Proprietary Name: | AGGRASTAT |
Non Proprietary Name: | TIROFIBAN |
Active Ingredient(s): | 5 mg/100mL & nbsp; TIROFIBAN |
Administration Route(s): | INTRAVENOUS |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 25208-002 |
Labeler Name: | Medicure International Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA020913 |
Marketing Category: | NDA |
Start Marketing Date: | 19980514 |
Package NDC: | 25208-002-02 |
Package Description: | 1 CONTAINER in 1 CARTON (25208-002-02) > 250 mL in 1 CONTAINER |
NDC Code | 25208-002-02 |
Proprietary Name | AGGRASTAT |
Package Description | 1 CONTAINER in 1 CARTON (25208-002-02) > 250 mL in 1 CONTAINER |
Product NDC | 25208-002 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | TIROFIBAN |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 19980514 |
Marketing Category Name | NDA |
Labeler Name | Medicure International Inc |
Substance Name | TIROFIBAN HYDROCHLORIDE |
Strength Number | 5 |
Strength Unit | mg/100mL |
Pharmaceutical Classes | Decreased Platelet Aggregation [PE],Platelet Aggregation Inhibitor [EPC] |