Visitor Monitoring Drug Details: URSO 250
 
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Drug Details

Drug Name: URSO 250
FDA Application No: (NDA) 020675
Active Ingredient(s): URSODIOL
Company: AXCAN SCANDIPHARM
Original Approval or Tentative Approval Date: December 10, 1997
Chemical Type: 3 New dosage form
Review Classification: S Standard review drug
O Orphan drug
 
 
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
URSO 250 URSODIOL250MGTABLET; ORAL Prescription No None
URSO FORTE URSODIOL500MGTABLET; ORAL Prescription Yes None


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