Visitor Monitoring Drug Details: PARCOPA
 
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Drug Details

Drug Name: PARCOPA
FDA Application No: (ANDA) 076699
Active Ingredient(s): CARBIDOPA; LEVODOPA
Company: SCHWARZ PHARMA
Original Approval or Tentative Approval Date: August 27, 2004
 
 
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
PARCOPA CARBIDOPA; LEVODOPA10MG; 100MGTABLET, ORALLY DISINTEGRATING; ORAL Prescription No None
PARCOPA CARBIDOPA; LEVODOPA25MG; 100MGTABLET, ORALLY DISINTEGRATING; ORAL Prescription No None
PARCOPA CARBIDOPA; LEVODOPA25MG; 250MGTABLET, ORALLY DISINTEGRATING; ORAL Prescription Yes None


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