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Aminocaproic Acid
Aminocaproic Acid - 61748-046-01 - (Aminocaproic Acid)
Drug Information of Aminocaproic Acid
| Product NDC: | 61748-046 |
| Proprietary Name: | Aminocaproic Acid |
| Non Proprietary Name: | Aminocaproic Acid |
| Active Ingredient(s): | 1000 mg/1 & nbsp; Aminocaproic Acid |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Aminocaproic Acid
| Product NDC: | 61748-046 |
| Labeler Name: | VersaPharm Incorporated |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA015197 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 20120601 |
Package Information of Aminocaproic Acid
| Package NDC: | 61748-046-01 |
| Package Description: | 100 TABLET in 1 BOTTLE (61748-046-01) |
NDC Information of Aminocaproic Acid
| NDC Code | 61748-046-01 |
| Proprietary Name | Aminocaproic Acid |
| Package Description | 100 TABLET in 1 BOTTLE (61748-046-01) |
| Product NDC | 61748-046 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Aminocaproic Acid |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20120601 |
| Marketing Category Name | NDA AUTHORIZED GENERIC |
| Labeler Name | VersaPharm Incorporated |
| Substance Name | AMINOCAPROIC ACID |
| Strength Number | 1000 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Antifibrinolytic Agent [EPC],Decreased Fibrinolysis [PE] |
