Product NDC: | 24987-447 |
Proprietary Name: | PARNATE |
Non Proprietary Name: | tranylcypromine sulfate |
Active Ingredient(s): | 10 mg/1 & nbsp; tranylcypromine sulfate |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, FILM COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 24987-447 |
Labeler Name: | Covis Pharmaceuticals Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA012342 |
Marketing Category: | NDA |
Start Marketing Date: | 20130114 |
Package NDC: | 24987-447-10 |
Package Description: | 100 TABLET, FILM COATED in 1 BOTTLE (24987-447-10) |
NDC Code | 24987-447-10 |
Proprietary Name | PARNATE |
Package Description | 100 TABLET, FILM COATED in 1 BOTTLE (24987-447-10) |
Product NDC | 24987-447 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | tranylcypromine sulfate |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 20130114 |
Marketing Category Name | NDA |
Labeler Name | Covis Pharmaceuticals Inc |
Substance Name | TRANYLCYPROMINE SULFATE |
Strength Number | 10 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Monoamine Oxidase Inhibitor [EPC],Monoamine Oxidase Inhibitors [MoA] |