Visitor Monitoring Drug Details: ACTIGALL
 
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Drug Details

Drug Name: ACTIGALL
FDA Application No: (NDA) 019594
Active Ingredient(s): URSODIOL
Company: WATSON PHARMS
Original Approval or Tentative Approval Date: December 31, 1987
Chemical Type: 1 New molecular entity (NME)
Review Classification: P Priority 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
ACTIGALL URSODIOL150MGCAPSULE; ORAL Discontinued No None
ACTIGALL URSODIOL300MGCAPSULE; ORAL Prescription Yes AB


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