| NDC Code | 63323-255-03 |
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| Package Description | 25 VIAL, SINGLE-DOSE in 1 TRAY (63323-255-03) / 1 mL in 1 VIAL, SINGLE-DOSE (63323-255-01) |
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| Product NDC | 63323-255 |
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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 | 20041130 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA040583 |
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| Manufacturer | Fresenius Kabi USA, LLC |
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| Substance Name | METHYLPREDNISOLONE SODIUM SUCCINATE |
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| Strength | 40 |
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| Strength Unit | mg/mL |
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| Pharmacy Classes | Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC] |
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