Visitor Monitoring Drug Details: PANRETIN
 
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Drug Details

Drug Name: PANRETIN
FDA Application No: (NDA) 020886
Active Ingredient(s): ALITRETINOIN
Company: EISAI MEDCL RES
Original Approval or Tentative Approval Date: February 2, 1999
Chemical Type: 1 New molecular entity (NME)
Review Classification: P Priority review drug
O Orphan drug
 
 
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Drug NameSort imageActive IngredientsStrengthDosage Form/RouteMarketing StatusRLDTE Code
PANRETIN ALITRETINOINEQ 0.1% BASEGEL; TOPICAL Prescription Yes None


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