| NDC Code | 25021-820-10 |
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| Package Description | 1 VIAL in 1 CARTON (25021-820-10) > 10 mL in 1 VIAL |
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| Product NDC | 25021-820 |
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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-ARTICULAR; INTRALESIONAL; INTRAMUSCULAR; INTRASYNOVIAL; SOFT TISSUE |
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| Start Marketing Date | 20211115 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA201835 |
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| Manufacturer | Sagent Pharmaceuticals |
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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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