Solu-Cortef is a Intramuscular; Intravenous Injection, Powder, For Solution in the Human Prescription Drug category. It is labeled and distributed by Pharmacia And Upjohn Company Llc. The primary component is Hydrocortisone Sodium Succinate.
Product ID | 0009-0825_4644d33c-93fd-4d77-b8d2-bb586f616c98 |
NDC | 0009-0825 |
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 | Pharmacia and Upjohn Company LLC |
Substance Name | HYDROCORTISONE SODIUM SUCCINATE |
Active Ingredient Strength | 100 mg/2mL |
Pharm Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
NDC Exclude Flag | N |
Listing Certified Through | 2020-12-31 |
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: | 65eefd58-b166-4d71-ade6-45c8fdf86922 |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI | |
UPC Code |
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 |