Solu-Cortef is a Intramuscular; Intravenous Injection, Powder, For Solution in the Human Prescription Drug category. It is labeled and distributed by Cardinal Health. The primary component is Hydrocortisone Sodium Succinate.
Product ID | 55154-3942_00185283-bb01-4b3b-95a9-70dddd2a0ee5 |
NDC | 55154-3942 |
Product Type | Human Prescription Drug |
Proprietary Name | Solu-Cortef |
Generic Name | Hydrocortisone Sodium Succinate |
Dosage Form | Injection, Powder, For Solution |
Route of Administration | INTRAMUSCULAR; INTRAVENOUS |
Marketing Start Date | 1955-04-27 |
Marketing Category | NDA / NDA |
Application Number | NDA009866 |
Labeler Name | Cardinal Health |
Substance Name | HYDROCORTISONE SODIUM SUCCINATE |
Active Ingredient Strength | 100 mg/2mL |
Pharm Classes | Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC] |
NDC Exclude Flag | N |
Listing Certified Through | 2023-12-31 |
Marketing Start Date | 1955-04-27 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | NDA |
Application Number | NDA009866 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 1955-04-27 |
Ingredient | Strength |
---|---|
HYDROCORTISONE SODIUM SUCCINATE | 100 mg/2mL |
SPL SET ID: | f5bb0854-a477-4e59-914b-eeeaef92a596 |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI |
NDC | Brand Name | Generic Name |
---|---|---|
0009-0005 | Solu-Cortef | hydrocortisone sodium succinate |
0009-0011 | Solu-Cortef | hydrocortisone sodium succinate |
0009-0013 | Solu-Cortef | hydrocortisone sodium succinate |
0009-0016 | Solu-Cortef | hydrocortisone sodium succinate |
0009-0825 | Solu-Cortef | hydrocortisone sodium succinate |
51662-1261 | SOLU-CORTEF | SOLU-CORTEF |
51662-1262 | SOLU-CORTEF | SOLU-CORTEF |
55154-3942 | Solu-Cortef | hydrocortisone sodium succinate |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
SOLU-CORTEF 71692184 0632542 Live/Registered |
UPJOHN COMPANY, THE 1955-07-29 |