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
 
There are no Therapeutic Equivalents Labels are not available
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
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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