NDC Code | 51662-1262-1 |
Package Description | 2 mL in 1 VIAL, SINGLE-DOSE (51662-1262-1) |
Product NDC | 51662-1262 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Solu-cortef |
Non-Proprietary Name | Solu-cortef |
Dosage Form | INJECTION, POWDER, FOR SOLUTION |
Usage | INTRAMUSCULAR; INTRAVENOUS |
Start Marketing Date | 20180903 |
Marketing Category Name | NDA |
Application Number | NDA009866 |
Manufacturer | HF Acquisition Co. LLC, DBA HealthFirst |
Substance Name | HYDROCORTISONE SODIUM SUCCINATE |
Strength | 250 |
Strength Unit | mg/2mL |
Pharmacy Classes | Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC] |