HYDROCORTISONE SODIUM SUCCINATE. Key specifications include physical_form: POWDER, administration: INTRAMUSCULAR OR INTRAVENOUS, primary_container_type: VIAL, SINGLE DOSE, protective_storage_feature: CONTROLLED ROOM TEMPERATURE, medical_designation_and_grade: UNITED STATES PHARMACOPEIA, active_medicament_medicinal_strength: 500.000 MILLIGRAMS HYDROCORTISONE EQUIVALENT. This product is currently in active production with full OEM support.
This part is cataloged in the Federal Logistics Information System (FLIS) under NSN 6505-01-588-5901, indicating validated use in U.S. government and defense logistics supply chains. Available through authorized enterprise resellers and TPM (Third Party Maintenance) channels.
Verify compatibility with your specific system configuration before ordering.
| physical_form | POWDER |
| administration | INTRAMUSCULAR OR INTRAVENOUS |
| primary_container_type | VIAL, SINGLE DOSE |
| protective_storage_feature | CONTROLLED ROOM TEMPERATURE |
| medical_designation_and_grade | UNITED STATES PHARMACOPEIA |
| active_medicament_medicinal_strength | 500.000 MILLIGRAMS HYDROCORTISONE EQUIVALENT |
| part_name_assigned_by_controlling_agency | SOLU CORTEF HYDROCORTISONE SODIUM SUCCINATE FOR INJECTION USP 500MG 4ML VIAL |
| NSN | 6505-01-588-5901 |
| PART NAME ASSIGNED BY CONTROLLING AGENCY | SOLU CORTEF HYDROCORTISONE SODIUM SUCCINATE FOR INJECTION USP 500MG 4ML VIAL |
| MEDICAL DESIGNATION AND GRADE | UNITED STATES PHARMACOPEIA |
| PHYSICAL FORM | POWDER |
| ADMINISTRATION | INTRAMUSCULAR OR INTRAVENOUS |
| SPECIAL FEATURES | WHEN MIXED, EACH 4 ML CONTAINS THE EQUIVALENT TO 500 MG HYDROCORTISONE; 4 ML VIAL; TRADE NAME: SOLU-CORTEF ACT-O-VIAL; SINGLE DOSE VIAL; PRESERVATIVE FREE; STORE AT CONTROLLED ROOM TEMPERATURE (68 DEG F TO 77 DEG F); DILUENT CONTAINED IN UPPER COMPARTMENT OF VIAL DEGF |
| ACTIVE MEDICAMENT MEDICINAL STRENGTH | 500.000 MILLIGRAMS HYDROCORTISONE EQUIVALENT |
| PRIMARY CONTAINER TYPE | VIAL, SINGLE DOSE |
| PROTECTIVE STORAGE FEATURE | CONTROLLED ROOM TEMPERATURE |