| Product NDC: | 66479-023 |
| Proprietary Name: | Amicar |
| Non Proprietary Name: | Aminocaproic Acid |
| Active Ingredient(s): | .25 g/mL & nbsp; Aminocaproic Acid |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 66479-023 |
| Labeler Name: | Xanodyne Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA015230 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20080930 |
| Package NDC: | 66479-023-56 |
| Package Description: | 473 mL in 1 BOTTLE (66479-023-56) |
| NDC Code | 66479-023-56 |
| Proprietary Name | Amicar |
| Package Description | 473 mL in 1 BOTTLE (66479-023-56) |
| Product NDC | 66479-023 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Aminocaproic Acid |
| Dosage Form Name | SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 20080930 |
| Marketing Category Name | NDA |
| Labeler Name | Xanodyne Pharmaceuticals, Inc. |
| Substance Name | AMINOCAPROIC ACID |
| Strength Number | .25 |
| Strength Unit | g/mL |
| Pharmaceutical Classes | Antifibrinolytic Agent [EPC],Decreased Fibrinolysis [PE] |