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Mycophenolate Mofetil - 0378-2250-05 - (mycophenolate mofetil)

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Drug Information of Mycophenolate Mofetil

Product NDC: 0378-2250
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: 0378-2250
Labeler Name: Mylan Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065520
Marketing Category: ANDA
Start Marketing Date: 20120904

Package Information of Mycophenolate Mofetil

Package NDC: 0378-2250-05
Package Description: 500 CAPSULE in 1 BOTTLE, PLASTIC (0378-2250-05)

NDC Information of Mycophenolate Mofetil

NDC Code 0378-2250-05
Proprietary Name Mycophenolate Mofetil
Package Description 500 CAPSULE in 1 BOTTLE, PLASTIC (0378-2250-05)
Product NDC 0378-2250
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name mycophenolate mofetil
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20120904
Marketing Category Name ANDA
Labeler Name Mylan Pharmaceuticals Inc.
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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