| NDC Code | 25021-810-30 |
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| Package Description | 1 VIAL in 1 CARTON (25021-810-30) > 16 mL in 1 VIAL |
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| Product NDC | 25021-810 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Methylprednisolone Sodium Succinate |
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| Non-Proprietary Name | Methylprednisolone Sodium Succinate |
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| Dosage Form | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
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| Usage | INTRAMUSCULAR; INTRAVENOUS |
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| Start Marketing Date | 20170315 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA040888 |
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| Manufacturer | Sagent Pharmaceuticals |
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| Substance Name | METHYLPREDNISOLONE SODIUM SUCCINATE |
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| Strength | 1 |
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| Strength Unit | g/16mL |
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| Pharmacy Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
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