| NDC Code | 55390-209-10 |
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| Package Description | 10 VIAL, SINGLE-DOSE in 1 BOX (55390-209-10) > 1 mL in 1 VIAL, SINGLE-DOSE |
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| Product NDC | 55390-209 |
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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 | 20070301 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA040662 |
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| Manufacturer | Bedford Laboratories |
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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 [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
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