| NDC Code | 42023-240-01 |
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| Package Description | 1 VIAL in 1 CARTON (42023-240-01) / 5 mL in 1 VIAL |
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| Product NDC | 42023-240 |
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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 | INTRA-ARTERIAL; INTRALESIONAL; INTRAMUSCULAR; SOFT TISSUE |
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| Start Marketing Date | 20220630 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA214297 |
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| Manufacturer | Endo USA, Inc. |
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| Substance Name | METHYLPREDNISOLONE ACETATE |
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| Strength | 80 |
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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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