Home
>
National Drug Code (NDC)
>
SOLU-CORTEF
SOLU-CORTEF - 55154-3925-5 - (hydrocortisone sodium succinate)
Drug Information of SOLU-CORTEF
| Product NDC: | 55154-3925 |
| Proprietary Name: | SOLU-CORTEF |
| Non Proprietary Name: | hydrocortisone sodium succinate |
| Active Ingredient(s): | 100 mg/2mL & nbsp; hydrocortisone sodium succinate |
| Administration Route(s): | INTRAMUSCULAR; INTRAVASCULAR |
| Dosage Form(s): | INJECTION, POWDER, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of SOLU-CORTEF
| Product NDC: | 55154-3925 |
| 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: | 55154-3925-5 |
| Package Description: | 5 VIAL, SINGLE-DOSE in 1 BAG (55154-3925-5) > 2 mL in 1 VIAL, SINGLE-DOSE |
NDC Information of SOLU-CORTEF
| NDC Code | 55154-3925-5 |
| Proprietary Name | SOLU-CORTEF |
| Package Description | 5 VIAL, SINGLE-DOSE in 1 BAG (55154-3925-5) > 2 mL in 1 VIAL, SINGLE-DOSE |
| Product NDC | 55154-3925 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | hydrocortisone sodium succinate |
| Dosage Form Name | INJECTION, POWDER, FOR SOLUTION |
| Route Name | INTRAMUSCULAR; INTRAVASCULAR |
| 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] |
