CellCept - 0004-0259-01 - (Mycophenolate Mofetil)

Alphabetical Index


Drug Information of CellCept

Product NDC: 0004-0259
Proprietary Name: CellCept
Non Proprietary Name: Mycophenolate Mofetil
Active Ingredient(s): 250    mg/1 & nbsp;   Mycophenolate Mofetil
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of CellCept

Product NDC: 0004-0259
Labeler Name: Genentech, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA050722
Marketing Category: NDA
Start Marketing Date: 19950503

Package Information of CellCept

Package NDC: 0004-0259-01
Package Description: 1 BOTTLE, PLASTIC in 1 CARTON (0004-0259-01) > 100 CAPSULE in 1 BOTTLE, PLASTIC

NDC Information of CellCept

NDC Code 0004-0259-01
Proprietary Name CellCept
Package Description 1 BOTTLE, PLASTIC in 1 CARTON (0004-0259-01) > 100 CAPSULE in 1 BOTTLE, PLASTIC
Product NDC 0004-0259
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Mycophenolate Mofetil
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 19950503
Marketing Category Name NDA
Labeler Name Genentech, Inc.
Substance Name MYCOPHENOLATE MOFETIL
Strength Number 250
Strength Unit mg/1
Pharmaceutical Classes Antimetabolite Immunosuppressant [EPC]

Complete Information of CellCept


General Information