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Angiomax
Angiomax - 65293-001-01 - (bivalirudin)
Drug Information of Angiomax
| Product NDC: | 65293-001 |
| Proprietary Name: | Angiomax |
| Non Proprietary Name: | bivalirudin |
| Active Ingredient(s): | 250 mg/5mL & nbsp; bivalirudin |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Angiomax
| Product NDC: | 65293-001 |
| Labeler Name: | The Medicines Company |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020873 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20001215 |
Package Information of Angiomax
| Package NDC: | 65293-001-01 |
| Package Description: | 10 VIAL, SINGLE-USE in 1 CARTON (65293-001-01) > 5 mL in 1 VIAL, SINGLE-USE |
NDC Information of Angiomax
| NDC Code | 65293-001-01 |
| Proprietary Name | Angiomax |
| Package Description | 10 VIAL, SINGLE-USE in 1 CARTON (65293-001-01) > 5 mL in 1 VIAL, SINGLE-USE |
| Product NDC | 65293-001 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | bivalirudin |
| Dosage Form Name | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20001215 |
| Marketing Category Name | NDA |
| Labeler Name | The Medicines Company |
| Substance Name | BIVALIRUDIN |
| Strength Number | 250 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes | Anti-coagulant [EPC],Direct Thrombin Inhibitor [EPC],Thrombin Inhibitors [MoA] |
