Visitor Monitoring Drug Details: ORAP
 
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Drug Details

Drug Name: ORAP
FDA Application No: (NDA) 017473
Active Ingredient(s): PIMOZIDE
Company: TEVA
Original Approval or Tentative Approval Date: July 31, 1984
Chemical Type: 1 New molecular entity (NME)
Review Classification: S Standard review drug
 
There are no Therapeutic Equivalents Labels are not available
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
ORAP PIMOZIDE2MGTABLET; ORAL Prescription Yes None
ORAP PIMOZIDE1MGTABLET; ORAL Prescription No None


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