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CORTEF
CORTEF - 0009-0044-01 - (hydrocortisone)
Drug Information of CORTEF
| Product NDC: | 0009-0044 |
| Proprietary Name: | CORTEF |
| Non Proprietary Name: | hydrocortisone |
| Active Ingredient(s): | 20 mg/1 & nbsp; hydrocortisone |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of CORTEF
| Product NDC: | 0009-0044 |
| Labeler Name: | Pharmacia and Upjohn Company |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA008697 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19521215 |
Package Information of CORTEF
| Package NDC: | 0009-0044-01 |
| Package Description: | 100 TABLET in 1 BOTTLE (0009-0044-01) |
NDC Information of CORTEF
| NDC Code | 0009-0044-01 |
| Proprietary Name | CORTEF |
| Package Description | 100 TABLET in 1 BOTTLE (0009-0044-01) |
| Product NDC | 0009-0044 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | hydrocortisone |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19521215 |
| Marketing Category Name | NDA |
| Labeler Name | Pharmacia and Upjohn Company |
| Substance Name | HYDROCORTISONE |
| Strength Number | 20 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
