Visitor Monitoring Drug Details: TEKTURNA
 
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Drug Details

Drug Name: TEKTURNA
FDA Application No: (NDA) 021985
Active Ingredient(s): ALISKIREN HEMIFUMARATE
Company: NOVARTIS
Original Approval or Tentative Approval Date: March 5, 2007
Chemical Type: 1 New molecular entity (NME)
Review Classification: S Standard review 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
TEKTURNA ALISKIREN HEMIFUMARATEEQ 150MG BASETABLET; ORAL Prescription No None
TEKTURNA ALISKIREN HEMIFUMARATEEQ 300MG BASETABLET; ORAL Prescription Yes None


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