| NDC Code | 51662-1261-1 |
|---|
| Package Description | 2 mL in 1 VIAL, SINGLE-DOSE (51662-1261-1) |
|---|
| Product NDC | 51662-1261 |
|---|
| 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 | 100 |
|---|
| Strength Unit | mg/2mL |
|---|
| Pharmacy Classes | Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC] |
|---|