| NDC Code | 51662-1695-3 |
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| Package Description | 25 POUCH in 1 CASE (51662-1695-3) / 1 VIAL, SINGLE-DOSE in 1 POUCH (51662-1695-2) / 2 mL in 1 VIAL, SINGLE-DOSE (51662-1695-1) |
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| Product NDC | 51662-1695 |
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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 |
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| Usage | INTRAVASCULAR; INTRAVENOUS |
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| Start Marketing Date | 20220324 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA212396 |
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| Manufacturer | HF Acquisition Co LLC, DBA HealthFirst |
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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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