| NDC Code | 71329-302-25 |
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| Package Description | 25 VIAL in 1 CARTON (71329-302-25) > 2 mL in 1 VIAL (71329-302-01) |
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| Product NDC | 71329-302 |
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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 |
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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 | 20210420 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA212396 |
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| Manufacturer | GeneYork Pharmaceuticals Group LLC |
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| Substance Name | METHYLPREDNISOLONE SODIUM SUCCINATE |
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| Strength | 125 |
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| Strength Unit | mg/2mL |
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| Pharmacy Classes | Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC] |
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