| NDC Code | 63323-265-30 |
|---|
| Package Description | 1 VIAL, MULTI-DOSE in 1 CARTON (63323-265-30) / 16 mL in 1 VIAL, MULTI-DOSE |
|---|
| Product NDC | 63323-265 |
|---|
| 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 | 20041130 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA040612 |
|---|
| Manufacturer | Fresenius Kabi USA, LLC |
|---|
| Substance Name | METHYLPREDNISOLONE SODIUM SUCCINATE |
|---|
| Strength | 1 |
|---|
| Strength Unit | g/16mL |
|---|
| Pharmacy Classes | Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC] |
|---|