Product NDC: | 76346-073 |
Proprietary Name: | Korlym |
Non Proprietary Name: | Mifepristone |
Active Ingredient(s): | 300 mg/1 & nbsp; Mifepristone |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 76346-073 |
Labeler Name: | Corcept Therapeutics Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA202107 |
Marketing Category: | NDA |
Start Marketing Date: | 20120217 |
Package NDC: | 76346-073-01 |
Package Description: | 28 TABLET in 1 BOTTLE (76346-073-01) |
NDC Code | 76346-073-01 |
Proprietary Name | Korlym |
Package Description | 28 TABLET in 1 BOTTLE (76346-073-01) |
Product NDC | 76346-073 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Mifepristone |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20120217 |
Marketing Category Name | NDA |
Labeler Name | Corcept Therapeutics Inc |
Substance Name | MIFEPRISTONE |
Strength Number | 300 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Progestational Hormone Receptor Antagonists [MoA],Progestin Antagonist [EPC] |