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NDC 00009-0013-05 Solu-Cortef 250 mg/2mL Details
Solu-Cortef 250 mg/2mL
Solu-Cortef is a INTRAMUSCULAR; INTRAVENOUS INJECTION, POWDER, FOR SOLUTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Pharmacia & Upjohn Company LLC. The primary component is HYDROCORTISONE SODIUM SUCCINATE.
MedlinePlus Drug Summary
Hydrocortisone injection is used to treat symptoms of low corticosteroid levels (lack of certain substances that are usually produced by the body and are needed for normal body functioning). It is also used to treat severe allergic reactions. Hydrocortisone injection is used in the management of multiple sclerosis (a disease in which the nerves do not function properly), lupus (a disease in which the body attacks many of its own organs), gastrointestinal disease, and certain types of arthritis. Hydrocortisone injection is also used to treat certain conditions that affect the blood, skin, eyes, nervous system, thyroid, kidneys, and lungs. Hydrocortisone injection is in a class of medications called corticosteroids. It works to treat people with low levels of corticosteroids by replacing steroids that are normally produced naturally by the body. It also works to treat other conditions by reducing swelling and redness and by changing the way the immune system works.
Related Packages: 00009-0013-05Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Hydrocortisone Injection
Product Information
| NDC | 00009-0013 |
|---|---|
| Product ID | 0009-0013_19af0443-b5c0-45bf-be08-1a5c06fd89f0 |
| Associated GPIs | 22100025402155 |
| GCN Sequence Number | 066111 |
| GCN Sequence Number Description | hydrocortisone sodium succ/PF VIAL 250 MG/2ML INJECTION |
| HIC3 | P5A |
| HIC3 Description | GLUCOCORTICOIDS |
| GCN | 28303 |
| HICL Sequence Number | 036875 |
| HICL Sequence Number Description | HYDROCORTISONE SODIUM SUCCINATE/PF |
| Brand/Generic | Brand |
| Proprietary Name | Solu-Cortef |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | hydrocortisone sodium succinate |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | INJECTION, POWDER, FOR SOLUTION |
| Route | INTRAMUSCULAR; INTRAVENOUS |
| Active Ingredient Strength | 250 |
| Active Ingredient Units | mg/2mL |
| Substance Name | HYDROCORTISONE SODIUM SUCCINATE |
| Labeler Name | Pharmacia & Upjohn Company LLC |
| Pharmaceutical Class | Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC] |
| DEA Schedule | n/a |
| Marketing Category | NDA |
| Application Number | NDA009866 |
| Listing Certified Through | 2025-12-31 |
Package
NDC 00009-0013-05 (00009001305)
| NDC Package Code | 0009-0013-05 |
|---|---|
| Billing NDC | 00009001305 |
| Package | 1 VIAL, SINGLE-DOSE in 1 CARTON (0009-0013-05) / 2 mL in 1 VIAL, SINGLE-DOSE |
| Marketing Start Date | 1955-04-27 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |