Visitor Monitoring Drug Details: JANUMET
 
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Drug Details

Drug Name: JANUMET
FDA Application No: (NDA) 022044
Active Ingredient(s): METFORMIN HYDROCHLORIDE; SITAGLIPTIN PHOSPHATE
Company: MERCK
Original Approval or Tentative Approval Date: March 30, 2007
Chemical Type: 4 New combination
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
JANUMET METFORMIN HYDROCHLORIDE; SITAGLIPTIN PHOSPHATE500MG; EQ 50MG BASETABLET; ORAL Prescription No None
JANUMET METFORMIN HYDROCHLORIDE; SITAGLIPTIN PHOSPHATE1GM; EQ 50MG BASETABLET; ORAL Prescription Yes None


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