Xeloda - 0004-1101-50 - (capecitabine)

Alphabetical Index


Drug Information of Xeloda

Product NDC: 0004-1101
Proprietary Name: Xeloda
Non Proprietary Name: capecitabine
Active Ingredient(s): 500    mg/1 & nbsp;   capecitabine
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Xeloda

Product NDC: 0004-1101
Labeler Name: Genentech, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020896
Marketing Category: NDA
Start Marketing Date: 19980430

Package Information of Xeloda

Package NDC: 0004-1101-50
Package Description: 120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0004-1101-50)

NDC Information of Xeloda

NDC Code 0004-1101-50
Proprietary Name Xeloda
Package Description 120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0004-1101-50)
Product NDC 0004-1101
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name capecitabine
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19980430
Marketing Category Name NDA
Labeler Name Genentech, Inc.
Substance Name CAPECITABINE
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes Nucleic Acid Synthesis Inhibitors [MoA],Nucleoside Metabolic Inhibitor [EPC]

Complete Information of Xeloda


General Information