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Mycophenolate Mofetil - 60505-2967-8 - (Mycophenolate Mofetil)

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Drug Information of Mycophenolate Mofetil

Product NDC: 60505-2967
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, COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Mycophenolate Mofetil

Product NDC: 60505-2967
Labeler Name: Apotex Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090499
Marketing Category: ANDA
Start Marketing Date: 20090504

Package Information of Mycophenolate Mofetil

Package NDC: 60505-2967-8
Package Description: 1000 TABLET, COATED in 1 BOTTLE (60505-2967-8)

NDC Information of Mycophenolate Mofetil

NDC Code 60505-2967-8
Proprietary Name Mycophenolate Mofetil
Package Description 1000 TABLET, COATED in 1 BOTTLE (60505-2967-8)
Product NDC 60505-2967
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Mycophenolate Mofetil
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 20090504
Marketing Category Name ANDA
Labeler Name Apotex Corp
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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