Visitor Monitoring Drug Details: REMODULIN
 
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Drug Details

Drug Name: REMODULIN
FDA Application No: (NDA) 021272
Active Ingredient(s): TREPROSTINIL SODIUM
Company: UNITED THERAP
Original Approval or Tentative Approval Date: May 21, 2002
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
REMODULIN TREPROSTINIL SODIUM1MG/MLINJECTABLE; IV (INFUSION)-SC Prescription No None
REMODULIN TREPROSTINIL SODIUM2.5MG/MLINJECTABLE; IV (INFUSION)-SC Prescription No None
REMODULIN TREPROSTINIL SODIUM5MG/MLINJECTABLE; IV (INFUSION)-SC Prescription No None
REMODULIN TREPROSTINIL SODIUM10MG/MLINJECTABLE; IV (INFUSION)-SC Prescription Yes None


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