| NDC Code | 0781-3522-70 |
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| Package Description | 1 VIAL, MULTI-DOSE in 1 CARTON (0781-3522-70) / 10 mL in 1 VIAL, MULTI-DOSE |
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| Product NDC | 0781-3522 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Methylprednisolone Acetate |
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| Non-Proprietary Name | Methylprednisolone Acetate |
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| Dosage Form | INJECTION, SUSPENSION |
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| Usage | INTRALESIONAL; INTRAMUSCULAR; INTRASYNOVIAL; SOFT TISSUE |
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| Start Marketing Date | 20240314 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA214870 |
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| Manufacturer | Sandoz Inc. |
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| Substance Name | METHYLPREDNISOLONE ACETATE |
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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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