Product NDC: | 61748-044 |
Proprietary Name: | Aminocaproic Acid |
Non Proprietary Name: | Aminocaproic Acid |
Active Ingredient(s): | .25 g/mL & nbsp; Aminocaproic Acid |
Administration Route(s): | ORAL |
Dosage Form(s): | SYRUP |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 61748-044 |
Labeler Name: | VersaPharm Incorporated |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA074759 |
Marketing Category: | ANDA |
Start Marketing Date: | 20000301 |
Package NDC: | 61748-044-08 |
Package Description: | 237 mL in 1 BOTTLE, PLASTIC (61748-044-08) |
NDC Code | 61748-044-08 |
Proprietary Name | Aminocaproic Acid |
Package Description | 237 mL in 1 BOTTLE, PLASTIC (61748-044-08) |
Product NDC | 61748-044 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Aminocaproic Acid |
Dosage Form Name | SYRUP |
Route Name | ORAL |
Start Marketing Date | 20000301 |
Marketing Category Name | ANDA |
Labeler Name | VersaPharm Incorporated |
Substance Name | AMINOCAPROIC ACID |
Strength Number | .25 |
Strength Unit | g/mL |
Pharmaceutical Classes | Antifibrinolytic Agent [EPC],Decreased Fibrinolysis [PE] |