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Mycophenolate Mofetil - 16729-019-16 - (Mycophenolate Mofetil)

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Drug Information of Mycophenolate Mofetil

Product NDC: 16729-019
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
Coding System: National Drug Codes(NDC)

Labeler Information of Mycophenolate Mofetil

Product NDC: 16729-019
Labeler Name: Accord Healthcare Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065416
Marketing Category: ANDA
Start Marketing Date: 20090504

Package Information of Mycophenolate Mofetil

Package NDC: 16729-019-16
Package Description: 500 TABLET in 1 BOTTLE (16729-019-16)

NDC Information of Mycophenolate Mofetil

NDC Code 16729-019-16
Proprietary Name Mycophenolate Mofetil
Package Description 500 TABLET in 1 BOTTLE (16729-019-16)
Product NDC 16729-019
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Mycophenolate Mofetil
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090504
Marketing Category Name ANDA
Labeler Name Accord Healthcare 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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