Angiomax is a Intravenous Injection, Powder, Lyophilized, For Solution in the Human Prescription Drug category. It is labeled and distributed by The Medicines Company. The primary component is Bivalirudin.
Product ID | 65293-001_3656c3c3-02e5-42cf-a73e-53a681d11340 |
NDC | 65293-001 |
Product Type | Human Prescription Drug |
Proprietary Name | Angiomax |
Generic Name | Bivalirudin |
Dosage Form | Injection, Powder, Lyophilized, For Solution |
Route of Administration | INTRAVENOUS |
Marketing Start Date | 2000-12-15 |
Marketing Category | NDA / NDA |
Application Number | NDA020873 |
Labeler Name | The Medicines Company |
Substance Name | BIVALIRUDIN |
Active Ingredient Strength | 250 mg/1 |
Pharm Classes | Anti-coagulant [EPC],Direct Thrombin Inhibitor [EPC],Thrombin Inhibitors [MoA] |
NDC Exclude Flag | N |
Listing Certified Through | 2020-12-31 |
Marketing Start Date | 2000-12-15 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | NDA |
Application Number | NDA020873 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2000-12-15 |
Ingredient | Strength |
---|---|
BIVALIRUDIN | 250 mg/1 |
SPL SET ID: | 911cd48f-01ea-4dec-b30c-95e7e0ea9d2a |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI | |
UPC Code |
NDC | Brand Name | Generic Name |
---|---|---|
0781-3447 | Angiomax | bivalirudin |
65293-001 | Angiomax | bivalirudin |
0409-8300 | Bivalirudin | BIVALIRUDIN |
0781-3158 | bivalirudin | bivalirudin |
0781-9158 | bivalirudin | bivalirudin |
16729-275 | Bivalirudin | Bivalirudin |
25021-405 | bivalirudin | bivalirudin |
52958-034 | Bivalirudin | Bivalirudin |
55111-652 | Bivalirudin | Bivalirudin |
55150-210 | BIVALIRUDIN | BIVALIRUDIN |
60505-6101 | Bivalirudin | bivalirudin |
63323-562 | Bivalirudin | Bivalirudin |
67457-256 | Bivalirudin | bivalirudin |
69097-601 | bivalirudin | bivalirudin |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
ANGIOMAX 75758548 2427591 Live/Registered |
SANDOZ INC. 1999-07-23 |