| NDC Code | 25021-808-10 |
|---|
| Package Description | 10 VIAL in 1 CARTON (25021-808-10) > 2 mL in 1 VIAL |
|---|
| Product NDC | 25021-808 |
|---|
| 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 | 20170315 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA040888 |
|---|
| Manufacturer | Sagent Pharmaceuticals |
|---|
| Substance Name | METHYLPREDNISOLONE SODIUM SUCCINATE |
|---|
| Strength | 125 |
|---|
| Strength Unit | mg/2mL |
|---|
| Pharmacy Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
|---|