Afinitor - 0078-0567-51 - (everolimus)

Alphabetical Index


Drug Information of Afinitor

Product NDC: 0078-0567
Proprietary Name: Afinitor
Non Proprietary Name: everolimus
Active Ingredient(s): 10    mg/1 & nbsp;   everolimus
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Afinitor

Product NDC: 0078-0567
Labeler Name: Novartis Pharmaceuticals Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA022334
Marketing Category: NDA
Start Marketing Date: 20090331

Package Information of Afinitor

Package NDC: 0078-0567-51
Package Description: 28 BLISTER PACK in 1 CARTON (0078-0567-51) > 1 TABLET in 1 BLISTER PACK (0078-0567-61)

NDC Information of Afinitor

NDC Code 0078-0567-51
Proprietary Name Afinitor
Package Description 28 BLISTER PACK in 1 CARTON (0078-0567-51) > 1 TABLET in 1 BLISTER PACK (0078-0567-61)
Product NDC 0078-0567
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name everolimus
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090331
Marketing Category Name NDA
Labeler Name Novartis Pharmaceuticals Corporation
Substance Name EVEROLIMUS
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Kinase Inhibitor [EPC],Protein Kinase Inhibitors [MoA]

Complete Information of Afinitor


General Information