High Outlier
Strength
360 mg/1
Manufacturer
Novartis Pharmaceuticals CorporationNDC
00078038666
Classification
Brand
Dosage Form
TABLET, DELAYED RELEASE
Route
ORAL
Last Updated
1/7/2026
Active Ingredients
MYCOPHENOLATE SODIUMApproval Type
New Drug (NDA)
FDA Application
NDA050791On Market Since
2/27/2004
Pharmacological Classes
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