| NDC Code | 0143-9182-01 |
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| Package Description | 1 VIAL, MULTI-DOSE in 1 CARTON (0143-9182-01) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, MULTI-DOSE |
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| Product NDC | 0143-9182 |
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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 | 20240115 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA202691 |
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| Manufacturer | Hikma Pharmaceuticals USA Inc. |
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| Substance Name | METHYLPREDNISOLONE SODIUM SUCCINATE |
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| Strength | 1 |
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| Strength Unit | g/1 |
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| Pharmacy Classes | Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC] |
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