Visitor Monitoring Drug Details: INCRELEX
 
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Drug Details

Drug Name: INCRELEX
FDA Application No: (NDA) 021839
Active Ingredient(s): MECASERMIN RECOMBINANT
Company: TERCICA
Original Approval or Tentative Approval Date: August 30, 2005
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
INCRELEX MECASERMIN RECOMBINANT40MG/4ML(10MG/ML)INJECTABLE; SUBCUTANEOUS Prescription Yes None


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