| NDC Code | 0009-0912-05 |
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| Package Description | 4 mL in 1 VIAL, SINGLE-DOSE (0009-0912-05) |
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| Product NDC | 0009-0912 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Solu-cortef |
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| Non-Proprietary Name | Hydrocortisone Sodium Succinate |
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| Dosage Form | INJECTION, POWDER, FOR SOLUTION |
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| Usage | INTRAMUSCULAR; INTRAVASCULAR |
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| Start Marketing Date | 19800427 |
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| End Marketing Date | 20140701 |
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| Marketing Category Name | NDA |
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| Application Number | NDA009866 |
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| Manufacturer | Pharmacia and Upjohn Company |
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| Substance Name | HYDROCORTISONE SODIUM SUCCINATE |
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| Strength | 500 |
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| Strength Unit | mg/4mL |
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| Pharmacy Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
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