| NDC Code | 70518-4345-0 |
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| Package Description | 25 VIAL, SINGLE-DOSE in 1 CARTON (70518-4345-0) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-DOSE (70518-4345-1) |
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| Product NDC | 70518-4345 |
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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, FOR SOLUTION |
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| Usage | INTRAMUSCULAR; INTRAVENOUS |
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| Start Marketing Date | 20250527 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA203125 |
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| Manufacturer | REMEDYREPACK INC. |
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| Substance Name | METHYLPREDNISOLONE SODIUM SUCCINATE |
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| Strength | 125 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC] |
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