Visitor Monitoring Drug Details: JANUVIA
 
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Drug Details

Drug Name: JANUVIA
FDA Application No: (NDA) 021995
Active Ingredient(s): SITAGLIPTIN PHOSPHATE
Company: MERCK CO INC
Original Approval or Tentative Approval Date: October 16, 2006
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
JANUVIA SITAGLIPTIN PHOSPHATEEQ 25MG BASETABLET; ORAL Prescription No None
JANUVIA SITAGLIPTIN PHOSPHATEEQ 50MG BASETABLET; ORAL Prescription No None
JANUVIA SITAGLIPTIN PHOSPHATEEQ 100MG BASETABLET; ORAL Prescription Yes None


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