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Mycophenolate Mofetil - 65841-681-05 - (Mycophenolate Mofetil)

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Drug Information of Mycophenolate Mofetil

Product NDC: 65841-681
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: 65841-681
Labeler Name: Cadila Healthcare Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065477
Marketing Category: ANDA
Start Marketing Date: 20090504

Package Information of Mycophenolate Mofetil

Package NDC: 65841-681-05
Package Description: 500 TABLET, FILM COATED in 1 BOTTLE (65841-681-05)

NDC Information of Mycophenolate Mofetil

NDC Code 65841-681-05
Proprietary Name Mycophenolate Mofetil
Package Description 500 TABLET, FILM COATED in 1 BOTTLE (65841-681-05)
Product NDC 65841-681
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Mycophenolate Mofetil
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20090504
Marketing Category Name ANDA
Labeler Name Cadila Healthcare Limited
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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