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Solu-Cortef
Solu-Cortef - 55154-3942-5 - (hydrocortisone sodium succinate)
Drug Information of Solu-Cortef
| Product NDC: | 55154-3942 |
| Proprietary Name: | Solu-Cortef |
| Non Proprietary Name: | hydrocortisone sodium succinate |
| Active Ingredient(s): | 100 mg/2mL & nbsp; hydrocortisone sodium succinate |
| Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS |
| Dosage Form(s): | INJECTION, POWDER, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Solu-Cortef
| Product NDC: | 55154-3942 |
| Labeler Name: | Cardinal Health |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA009866 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19550427 |
Package Information of Solu-Cortef
| Package NDC: | 55154-3942-5 |
| Package Description: | 5 VIAL, SINGLE-DOSE in 1 BAG (55154-3942-5) > 2 mL in 1 VIAL, SINGLE-DOSE |
NDC Information of Solu-Cortef
| NDC Code | 55154-3942-5 |
| Proprietary Name | Solu-Cortef |
| Package Description | 5 VIAL, SINGLE-DOSE in 1 BAG (55154-3942-5) > 2 mL in 1 VIAL, SINGLE-DOSE |
| Product NDC | 55154-3942 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | hydrocortisone sodium succinate |
| Dosage Form Name | INJECTION, POWDER, FOR SOLUTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS |
| Start Marketing Date | 19550427 |
| Marketing Category Name | NDA |
| Labeler Name | Cardinal Health |
| Substance Name | HYDROCORTISONE SODIUM SUCCINATE |
| Strength Number | 100 |
| Strength Unit | mg/2mL |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
