| NDC Code | 70710-1907-1 |
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| Package Description | 1 VIAL in 1 CARTON (70710-1907-1) / 2 mL in 1 VIAL |
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| Product NDC | 70710-1907 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Hydrocortisone Sodium Succinate |
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| Non-Proprietary Name | Hydrocortisone Sodium Succinate |
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| Dosage Form | INJECTION |
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| Usage | INTRAMUSCULAR; INTRAVENOUS |
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| Start Marketing Date | 20260509 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA217191 |
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| Manufacturer | Zydus Pharmaceuticals USA Inc. |
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| Substance Name | HYDROCORTISONE SODIUM SUCCINATE |
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| Strength | 100 |
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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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