Product NDC: | 49411-052 |
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: | 49411-052 |
Labeler Name: | Clover Pharmaceuticals Corp. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA015230 |
Marketing Category: | NDA |
Start Marketing Date: | 20120411 |
Package NDC: | 49411-052-16 |
Package Description: | 473 mL in 1 BOTTLE (49411-052-16) |
NDC Code | 49411-052-16 |
Proprietary Name | AMICAR |
Package Description | 473 mL in 1 BOTTLE (49411-052-16) |
Product NDC | 49411-052 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Aminocaproic Acid |
Dosage Form Name | SOLUTION |
Route Name | ORAL |
Start Marketing Date | 20120411 |
Marketing Category Name | NDA |
Labeler Name | Clover Pharmaceuticals Corp. |
Substance Name | AMINOCAPROIC ACID |
Strength Number | .25 |
Strength Unit | g/mL |
Pharmaceutical Classes | Antifibrinolytic Agent [EPC],Decreased Fibrinolysis [PE] |