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Cosyntropin
Cosyntropin - 0781-3440-95 - (Cosyntropin)
Drug Information of Cosyntropin
| Product NDC: | 0781-3440 |
| Proprietary Name: | Cosyntropin |
| Non Proprietary Name: | Cosyntropin |
| Active Ingredient(s): | .25 mg/mL & nbsp; Cosyntropin |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Cosyntropin
| Product NDC: | 0781-3440 |
| Labeler Name: | Sandoz Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA202147 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120629 |
Package Information of Cosyntropin
| Package NDC: | 0781-3440-95 |
| Package Description: | 10 VIAL in 1 CARTON (0781-3440-95) > 1 mL in 1 VIAL (0781-3440-71) |
NDC Information of Cosyntropin
| NDC Code | 0781-3440-95 |
| Proprietary Name | Cosyntropin |
| Package Description | 10 VIAL in 1 CARTON (0781-3440-95) > 1 mL in 1 VIAL (0781-3440-71) |
| Product NDC | 0781-3440 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Cosyntropin |
| Dosage Form Name | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20120629 |
| Marketing Category Name | ANDA |
| Labeler Name | Sandoz Inc |
| Substance Name | COSYNTROPIN |
| Strength Number | .25 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Adrenocorticotropic Hormone [Chemical/Ingredient],Adrenocorticotropic Hormone [EPC] |
