Visitor Monitoring Drug Details: ACTHAR
 
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Drug Details

Drug Name: ACTHAR
FDA Application No: (NDA) 007504
Active Ingredient(s): CORTICOTROPIN
Company: SANOFI AVENTIS US
Original Approval or Tentative Approval Date: July 3, 1950
Chemical Type: 1 New molecular entity (NME)
Review Classification: P Priority review drug
 
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
ACTHAR CORTICOTROPIN25 UNITS/VIALINJECTABLE; INJECTION Discontinued No None
ACTHAR CORTICOTROPIN40 UNITS/VIALINJECTABLE; INJECTION Discontinued No None


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