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Cortrosyn
Cortrosyn - 0548-5900-00 - (Cosyntropin)
Drug Information of Cortrosyn
| Product NDC: | 0548-5900 |
| Proprietary Name: | Cortrosyn |
| Non Proprietary Name: | Cosyntropin |
| Active Ingredient(s): | .25 mg/mL & nbsp; Cosyntropin |
| Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS |
| Dosage Form(s): | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Cortrosyn
| Product NDC: | 0548-5900 |
| Labeler Name: | Amphastar Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA016750 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20030801 |
Package Information of Cortrosyn
| Package NDC: | 0548-5900-00 |
| Package Description: | 10 VIAL in 1 CARTON (0548-5900-00) > 1 mL in 1 VIAL |
NDC Information of Cortrosyn
| NDC Code | 0548-5900-00 |
| Proprietary Name | Cortrosyn |
| Package Description | 10 VIAL in 1 CARTON (0548-5900-00) > 1 mL in 1 VIAL |
| Product NDC | 0548-5900 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Cosyntropin |
| Dosage Form Name | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS |
| Start Marketing Date | 20030801 |
| Marketing Category Name | NDA |
| Labeler Name | Amphastar Pharmaceuticals, Inc. |
| Substance Name | COSYNTROPIN |
| Strength Number | .25 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Adrenocorticotropic Hormone [Chemical/Ingredient],Adrenocorticotropic Hormone [EPC] |
