CellCept - 49999-937-60 - (Mycophenolate Mofetil)

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Drug Information of CellCept

Product NDC: 49999-937
Proprietary Name: CellCept
Non Proprietary Name: Mycophenolate Mofetil
Active Ingredient(s): 500    mg/1 & nbsp;   Mycophenolate Mofetil
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of CellCept

Product NDC: 49999-937
Labeler Name: Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA050723
Marketing Category: NDA
Start Marketing Date: 19970619

Package Information of CellCept

Package NDC: 49999-937-60
Package Description: 60 TABLET, FILM COATED in 1 BOTTLE (49999-937-60)

NDC Information of CellCept

NDC Code 49999-937-60
Proprietary Name CellCept
Package Description 60 TABLET, FILM COATED in 1 BOTTLE (49999-937-60)
Product NDC 49999-937
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Mycophenolate Mofetil
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19970619
Marketing Category Name NDA
Labeler Name Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Substance Name MYCOPHENOLATE MOFETIL
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes Antimetabolite Immunosuppressant [EPC]

Complete Information of CellCept


General Information