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Mycophenolate Mofetil - 0093-7477-01 - (Mycophenolate Mofetil)

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Drug Information of Mycophenolate Mofetil

Product NDC: 0093-7477
Proprietary Name: Mycophenolate Mofetil
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 Mycophenolate Mofetil

Product NDC: 0093-7477
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065457
Marketing Category: ANDA
Start Marketing Date: 20090505

Package Information of Mycophenolate Mofetil

Package NDC: 0093-7477-01
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE (0093-7477-01)

NDC Information of Mycophenolate Mofetil

NDC Code 0093-7477-01
Proprietary Name Mycophenolate Mofetil
Package Description 100 TABLET, FILM COATED in 1 BOTTLE (0093-7477-01)
Product NDC 0093-7477
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Mycophenolate Mofetil
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20090505
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA Inc
Substance Name MYCOPHENOLATE MOFETIL
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes Antimetabolite Immunosuppressant [EPC]

Complete Information of Mycophenolate Mofetil


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