NDC Code | 55150-264-20 |
Package Description | 1 VIAL, MULTI-DOSE in 1 CARTON (55150-264-20) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, MULTI-DOSE |
Product NDC | 55150-264 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Methylprednisolone Sodium Succinate |
Non-Proprietary Name | Methylprednisolone Sodium Succinate |
Dosage Form | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
Usage | INTRAMUSCULAR; INTRAVENOUS |
Start Marketing Date | 20151215 |
Marketing Category Name | ANDA |
Application Number | ANDA207667 |
Manufacturer | Eugia US LLC |
Substance Name | METHYLPREDNISOLONE SODIUM SUCCINATE |
Strength | 500 |
Strength Unit | mg/1 |
Pharmacy Classes | Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC] |