Visitor Monitoring Drug Details: SANDIMMUNE
 
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Drug Details

Drug Name: SANDIMMUNE
FDA Application No: (NDA) 050625
Active Ingredient(s): CYCLOSPORINE
Company: NOVARTIS
Original Approval or Tentative Approval Date: March 2, 1990
Chemical Type: 3 New dosage form
Review Classification: P Priority review drug
 
Therapeutic Equivalents Label Information
Approval History, Letters, Reviews and Related Documents
 
You can see the products in the same application. The table can be sorted by clicking the header columns.
 
Drug NameSort imageActive IngredientsStrengthDosage Form/RouteMarketing StatusRLDTE Code
SANDIMMUNE CYCLOSPORINE25MGCAPSULE; ORAL Prescription No AB2
SANDIMMUNE CYCLOSPORINE100MGCAPSULE; ORAL Prescription Yes AB2
SANDIMMUNE CYCLOSPORINE50MGCAPSULE; ORAL Prescription No BX


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