Visitor Monitoring Drug Details: NEORAL
 
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Drug Details

Drug Name: NEORAL
FDA Application No: (NDA) 050715
Active Ingredient(s): CYCLOSPORINE
Company: NOVARTIS
Original Approval or Tentative Approval Date: July 14, 1995
Chemical Type: 3 New dosage form
Review Classification: S Standard 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
NEORAL CYCLOSPORINE25MGCAPSULE; ORAL Prescription No AB1
NEORAL CYCLOSPORINE100MGCAPSULE; ORAL Prescription Yes AB1
NEORAL CYCLOSPORINE50MGCAPSULE; ORAL Discontinued No None


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