Product NDC: | 0078-0592 |
Proprietary Name: | Tasigna |
Non Proprietary Name: | nilotinib |
Active Ingredient(s): | 150 mg/1 & nbsp; nilotinib |
Administration Route(s): | ORAL |
Dosage Form(s): | CAPSULE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0078-0592 |
Labeler Name: | Novartis Pharmaceuticals Corporation |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA022068 |
Marketing Category: | NDA |
Start Marketing Date: | 20071029 |
Package NDC: | 0078-0592-87 |
Package Description: | 4 BLISTER PACK in 1 CARTON (0078-0592-87) > 28 CAPSULE in 1 BLISTER PACK |
NDC Code | 0078-0592-87 |
Proprietary Name | Tasigna |
Package Description | 4 BLISTER PACK in 1 CARTON (0078-0592-87) > 28 CAPSULE in 1 BLISTER PACK |
Product NDC | 0078-0592 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | nilotinib |
Dosage Form Name | CAPSULE |
Route Name | ORAL |
Start Marketing Date | 20071029 |
Marketing Category Name | NDA |
Labeler Name | Novartis Pharmaceuticals Corporation |
Substance Name | NILOTINIB |
Strength Number | 150 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Kinase Inhibitor [EPC],Protein Kinase Inhibitors [MoA] |