Product NDC: | 0078-0469 |
Proprietary Name: | Exjade |
Non Proprietary Name: | deferasirox |
Active Ingredient(s): | 250 mg/1 & nbsp; deferasirox |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, FOR SUSPENSION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0078-0469 |
Labeler Name: | Novartis Pharmaceuticals Corporation |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA021882 |
Marketing Category: | NDA |
Start Marketing Date: | 20051130 |
Package NDC: | 0078-0469-15 |
Package Description: | 30 TABLET, FOR SUSPENSION in 1 BOTTLE (0078-0469-15) |
NDC Code | 0078-0469-15 |
Proprietary Name | Exjade |
Package Description | 30 TABLET, FOR SUSPENSION in 1 BOTTLE (0078-0469-15) |
Product NDC | 0078-0469 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | deferasirox |
Dosage Form Name | TABLET, FOR SUSPENSION |
Route Name | ORAL |
Start Marketing Date | 20051130 |
Marketing Category Name | NDA |
Labeler Name | Novartis Pharmaceuticals Corporation |
Substance Name | DEFERASIROX |
Strength Number | 250 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Iron Chelating Activity [MoA],Iron Chelator [EPC] |