| NDC Code | 51662-1483-1 |
|---|
| Package Description | 1 VIAL in 1 CARTON (51662-1483-1) > 4 mL in 1 VIAL |
|---|
| Product NDC | 51662-1483 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Solu-medrol(r) Methylprednisolone Sodium Succinat |
|---|
| Non-Proprietary Name | Solu-medrol(r) Methylprednisolone Sodium Succinat |
|---|
| Dosage Form | INJECTION, POWDER, FOR SOLUTION |
|---|
| Usage | INTRAMUSCULAR; INTRAVENOUS |
|---|
| Start Marketing Date | 20191214 |
|---|
| Marketing Category Name | NDA |
|---|
| Application Number | NDA011856 |
|---|
| Manufacturer | HF Acquisition Co LLC, DBA HealthFirst |
|---|
| Substance Name | METHYLPREDNISOLONE SODIUM SUCCINATE |
|---|
| Strength | 500 |
|---|
| Strength Unit | mg/4mL |
|---|
| Pharmacy Classes | Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC] |
|---|