Visitor Monitoring Drug Details: SINEMET
 
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Drug Details

Drug Name: SINEMET
FDA Application No: (NDA) 017555
Active Ingredient(s): CARBIDOPA; LEVODOPA
Company: BRISTOL MYERS SQUIBB
Original Approval or Tentative Approval Date: May 2, 1975
Chemical Type: 14 New molecular entity and new combination
Review Classification: P Priority 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
SINEMET CARBIDOPA; LEVODOPA10MG; 100MGTABLET; ORAL Prescription No AB
SINEMET CARBIDOPA; LEVODOPA25MG; 250MGTABLET; ORAL Prescription Yes AB
SINEMET CARBIDOPA; LEVODOPA25MG; 100MGTABLET; ORAL Prescription No AB


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