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A-HYDROCORT
A-HYDROCORT - 0409-4856-05 - (HYDROCORTISONE SODIUM SUCCINATE)
Drug Information of A-HYDROCORT
| Product NDC: | 0409-4856 |
| Proprietary Name: | A-HYDROCORT |
| Non Proprietary Name: | HYDROCORTISONE SODIUM SUCCINATE |
| Active Ingredient(s): | 100 mg/2mL & nbsp; HYDROCORTISONE SODIUM SUCCINATE |
| Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS |
| Dosage Form(s): | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of A-HYDROCORT
| Product NDC: | 0409-4856 |
| Labeler Name: | Hospira, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040666 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110512 |
Package Information of A-HYDROCORT
| Package NDC: | 0409-4856-05 |
| Package Description: | 10 VIAL, SINGLE-DOSE in 1 CARTON (0409-4856-05) > 2 mL in 1 VIAL, SINGLE-DOSE |
NDC Information of A-HYDROCORT
| NDC Code | 0409-4856-05 |
| Proprietary Name | A-HYDROCORT |
| Package Description | 10 VIAL, SINGLE-DOSE in 1 CARTON (0409-4856-05) > 2 mL in 1 VIAL, SINGLE-DOSE |
| Product NDC | 0409-4856 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | HYDROCORTISONE SODIUM SUCCINATE |
| Dosage Form Name | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS |
| Start Marketing Date | 20110512 |
| Marketing Category Name | ANDA |
| Labeler Name | Hospira, Inc. |
| Substance Name | HYDROCORTISONE SODIUM SUCCINATE |
| Strength Number | 100 |
| Strength Unit | mg/2mL |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
