Zortress - 0078-0415-20 - (everolimus)

Alphabetical Index


Drug Information of Zortress

Product NDC: 0078-0415
Proprietary Name: Zortress
Non Proprietary Name: everolimus
Active Ingredient(s): .75    mg/1 & nbsp;   everolimus
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Zortress

Product NDC: 0078-0415
Labeler Name: Novartis Pharmaceuticals Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021560
Marketing Category: NDA
Start Marketing Date: 20100422

Package Information of Zortress

Package NDC: 0078-0415-20
Package Description: 60 BLISTER PACK in 1 BOX (0078-0415-20) > 1 TABLET in 1 BLISTER PACK (0078-0415-61)

NDC Information of Zortress

NDC Code 0078-0415-20
Proprietary Name Zortress
Package Description 60 BLISTER PACK in 1 BOX (0078-0415-20) > 1 TABLET in 1 BLISTER PACK (0078-0415-61)
Product NDC 0078-0415
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name everolimus
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100422
Marketing Category Name NDA
Labeler Name Novartis Pharmaceuticals Corporation
Substance Name EVEROLIMUS
Strength Number .75
Strength Unit mg/1
Pharmaceutical Classes Kinase Inhibitor [EPC],Protein Kinase Inhibitors [MoA]

Complete Information of Zortress


General Information