SPRYCEL - 0003-0524-11 - (dasatinib)

Alphabetical Index


Drug Information of SPRYCEL

Product NDC: 0003-0524
Proprietary Name: SPRYCEL
Non Proprietary Name: dasatinib
Active Ingredient(s): 70    mg/1 & nbsp;   dasatinib
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of SPRYCEL

Product NDC: 0003-0524
Labeler Name: E.R. Squibb & Sons, L.L.C.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021986
Marketing Category: NDA
Start Marketing Date: 20060627

Package Information of SPRYCEL

Package NDC: 0003-0524-11
Package Description: 1 BOTTLE in 1 CARTON (0003-0524-11) > 60 TABLET in 1 BOTTLE

NDC Information of SPRYCEL

NDC Code 0003-0524-11
Proprietary Name SPRYCEL
Package Description 1 BOTTLE in 1 CARTON (0003-0524-11) > 60 TABLET in 1 BOTTLE
Product NDC 0003-0524
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name dasatinib
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20060627
Marketing Category Name NDA
Labeler Name E.R. Squibb & Sons, L.L.C.
Substance Name DASATINIB
Strength Number 70
Strength Unit mg/1
Pharmaceutical Classes Kinase Inhibitor [EPC],Protein Kinase Inhibitors [MoA]

Complete Information of SPRYCEL


General Information