Visitor Monitoring Drug Details: PARADIONE
 
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Drug Details

Drug Name: PARADIONE
FDA Application No: (NDA) 006800
Active Ingredient(s): PARAMETHADIONE
Company: ABBOTT
Original Approval or Tentative Approval Date: June 15, 1949
 
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
PARADIONE PARAMETHADIONE300MGCAPSULE; ORAL Discontinued No None
PARADIONE PARAMETHADIONE300MG/MLSOLUTION; ORAL Discontinued No None
PARADIONE PARAMETHADIONE150MGCAPSULE; ORAL Discontinued No None


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