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
 
There are no Therapeutic Equivalents Label Information
Approval History, Letters, Reviews and Related Documents
 
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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