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Aminocaproic Acid
Aminocaproic Acid - 0517-9120-25 - (Aminocaproic Acid)
Drug Information of Aminocaproic Acid
| Product NDC: | 0517-9120 |
| Proprietary Name: | Aminocaproic Acid |
| Non Proprietary Name: | Aminocaproic Acid |
| Active Ingredient(s): | 250 mg/mL & nbsp; Aminocaproic Acid |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Aminocaproic Acid
| Product NDC: | 0517-9120 |
| Labeler Name: | American Regent, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA071192 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19900930 |
Package Information of Aminocaproic Acid
| Package NDC: | 0517-9120-25 |
| Package Description: | 25 VIAL, MULTI-DOSE in 1 TRAY (0517-9120-25) > 20 mL in 1 VIAL, MULTI-DOSE |
NDC Information of Aminocaproic Acid
| NDC Code | 0517-9120-25 |
| Proprietary Name | Aminocaproic Acid |
| Package Description | 25 VIAL, MULTI-DOSE in 1 TRAY (0517-9120-25) > 20 mL in 1 VIAL, MULTI-DOSE |
| Product NDC | 0517-9120 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Aminocaproic Acid |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 19900930 |
| Marketing Category Name | ANDA |
| Labeler Name | American Regent, Inc. |
| Substance Name | AMINOCAPROIC ACID |
| Strength Number | 250 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Antifibrinolytic Agent [EPC],Decreased Fibrinolysis [PE] |
