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SOLU-CORTEF
SOLU-CORTEF - 0009-0920-03 - (HYDROCORTISONE SODIUM SUCCINATE)
Drug Information of SOLU-CORTEF
| Product NDC: | 0009-0920 |
| Proprietary Name: | SOLU-CORTEF |
| Non Proprietary Name: | HYDROCORTISONE SODIUM SUCCINATE |
| Active Ingredient(s): | 1000 mg/8mL & nbsp; HYDROCORTISONE SODIUM SUCCINATE |
| Administration Route(s): | INTRAMUSCULAR; INTRAVASCULAR |
| Dosage Form(s): | INJECTION, POWDER, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of SOLU-CORTEF
| Product NDC: | 0009-0920 |
| Labeler Name: | Pharmacia and Upjohn Company |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA009866 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19550427 |
Package Information of SOLU-CORTEF
| Package NDC: | 0009-0920-03 |
| Package Description: | 8 mL in 1 VIAL, SINGLE-DOSE (0009-0920-03) |
NDC Information of SOLU-CORTEF
| NDC Code | 0009-0920-03 |
| Proprietary Name | SOLU-CORTEF |
| Package Description | 8 mL in 1 VIAL, SINGLE-DOSE (0009-0920-03) |
| Product NDC | 0009-0920 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | HYDROCORTISONE SODIUM SUCCINATE |
| Dosage Form Name | INJECTION, POWDER, FOR SOLUTION |
| Route Name | INTRAMUSCULAR; INTRAVASCULAR |
| Start Marketing Date | 19550427 |
| Marketing Category Name | NDA |
| Labeler Name | Pharmacia and Upjohn Company |
| Substance Name | HYDROCORTISONE SODIUM SUCCINATE |
| Strength Number | 1000 |
| Strength Unit | mg/8mL |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
