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Mycophenolate Mofetil - 55154-6262-0 - (mycophenolate mofetil)

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Drug Information of Mycophenolate Mofetil

Product NDC: 55154-6262
Proprietary Name: Mycophenolate Mofetil
Non Proprietary Name: mycophenolate mofetil
Active Ingredient(s): 250    mg/1 & nbsp;   mycophenolate mofetil
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Mycophenolate Mofetil

Product NDC: 55154-6262
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065520
Marketing Category: ANDA
Start Marketing Date: 20111025

Package Information of Mycophenolate Mofetil

Package NDC: 55154-6262-0
Package Description: 10 BLISTER PACK in 1 BAG (55154-6262-0) > 1 CAPSULE in 1 BLISTER PACK

NDC Information of Mycophenolate Mofetil

NDC Code 55154-6262-0
Proprietary Name Mycophenolate Mofetil
Package Description 10 BLISTER PACK in 1 BAG (55154-6262-0) > 1 CAPSULE in 1 BLISTER PACK
Product NDC 55154-6262
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name mycophenolate mofetil
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20111025
Marketing Category Name ANDA
Labeler Name Cardinal Health
Substance Name MYCOPHENOLATE MOFETIL
Strength Number 250
Strength Unit mg/1
Pharmaceutical Classes Antimetabolite Immunosuppressant [EPC]

Complete Information of Mycophenolate Mofetil


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