Home
>
National Drug Code (NDC)
>
Tranexamic Acid
Tranexamic Acid - 0517-0960-10 - (Tranexamic Acid)
Drug Information of Tranexamic Acid
| Product NDC: | 0517-0960 |
| Proprietary Name: | Tranexamic Acid |
| Non Proprietary Name: | Tranexamic Acid |
| Active Ingredient(s): | 100 mg/mL & nbsp; Tranexamic Acid |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Tranexamic Acid
| Product NDC: | 0517-0960 |
| Labeler Name: | American Regent, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA201885 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20111115 |
Package Information of Tranexamic Acid
| Package NDC: | 0517-0960-10 |
| Package Description: | 10 VIAL, GLASS in 1 CARTON (0517-0960-10) > 10 mL in 1 VIAL, GLASS (0517-0960-01) |
NDC Information of Tranexamic Acid
| NDC Code | 0517-0960-10 |
| Proprietary Name | Tranexamic Acid |
| Package Description | 10 VIAL, GLASS in 1 CARTON (0517-0960-10) > 10 mL in 1 VIAL, GLASS (0517-0960-01) |
| Product NDC | 0517-0960 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Tranexamic Acid |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20111115 |
| Marketing Category Name | ANDA |
| Labeler Name | American Regent, Inc. |
| Substance Name | TRANEXAMIC ACID |
| Strength Number | 100 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Antifibrinolytic Agent [EPC],Decreased Fibrinolysis [PE] |
