Visitor Monitoring Drug Details: LARODOPA
 
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Drug Details

Drug Name: LARODOPA
FDA Application No: (NDA) 016912
Active Ingredient(s): LEVODOPA
Company: ROCHE
Original Approval or Tentative Approval Date: June 4, 1970
Chemical Type: 1 New molecular entity (NME)
Review Classification: P Priority review drug
 
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
LARODOPA LEVODOPA250MGCAPSULE; ORAL Discontinued No None
LARODOPA LEVODOPA100MGCAPSULE; ORAL Discontinued No None
LARODOPA LEVODOPA250MGTABLET; ORAL Discontinued No None
LARODOPA LEVODOPA500MGTABLET; ORAL Discontinued No None
LARODOPA LEVODOPA100MGTABLET; ORAL Discontinued No None
LARODOPA LEVODOPA500MGCAPSULE; ORAL Discontinued No None


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