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Product Detail

National Drug Code
60505-2965
11 Digit NDC Code
60505-2965-6
Type
HUMAN PRESCRIPTION DRUG
Proprietary Name
Mycophenolic Acid
Proprietary Name Suffix
Non-Proprietary Name
Mycophenolic Acid
Package Description
60 TABLET, DELAYED RELEASE in 1 BOTTLE (60505-2965-6)
Dosage Form
TABLET, DELAYED RELEASE
Route of Administration
ORAL
Start Marketing
8/21/2012
End Marketing
6/30/2021
Marketing Category
ANDA
Application Number
ANDA091558
Labeler
Apotex Corp  
Active Ingredients
  • MYCOPHENOLATE SODIUM 180mg/1
Pharmacological Classes
Antimetabolite Immunosuppressant [EPC]
DEA Schedule

Additional Packages

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NDC Database last updated 12/18/2020

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