Product NDC: | 0003-0852 |
Proprietary Name: | SPRYCEL |
Non Proprietary Name: | dasatinib |
Active Ingredient(s): | 100 mg/1 & nbsp; dasatinib |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0003-0852 |
Labeler Name: | E.R. Squibb & Sons, L.L.C. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA021986 |
Marketing Category: | NDA |
Start Marketing Date: | 20080530 |
Package NDC: | 0003-0852-22 |
Package Description: | 1 BOTTLE in 1 CARTON (0003-0852-22) > 30 TABLET in 1 BOTTLE |
NDC Code | 0003-0852-22 |
Proprietary Name | SPRYCEL |
Package Description | 1 BOTTLE in 1 CARTON (0003-0852-22) > 30 TABLET in 1 BOTTLE |
Product NDC | 0003-0852 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | dasatinib |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20080530 |
Marketing Category Name | NDA |
Labeler Name | E.R. Squibb & Sons, L.L.C. |
Substance Name | DASATINIB |
Strength Number | 100 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Kinase Inhibitor [EPC],Protein Kinase Inhibitors [MoA] |