Visitor Monitoring Drug Details: BENDECTIN
 
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Drug Details

Drug Name: BENDECTIN
FDA Application No: (NDA) 010598
Active Ingredient(s): DOXYLAMINE SUCCINATE; PYRIDOXINE HYDROCHLORIDE
Company: SANOFI AVENTIS US
Original Approval or Tentative Approval Date: July 30, 1956
Chemical Type: 4 New combination
Review Classification: S Standard review drug
 
There are no Therapeutic Equivalents Labels are not available
Approval History, Letters, Reviews and Related Documents
 
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Drug NameSort imageActive IngredientsStrengthDosage Form/RouteMarketing StatusRLDTE Code
BENDECTIN DOXYLAMINE SUCCINATE; PYRIDOXINE HYDROCHLORIDE10MG; 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**TABLET, EXTENDED RELEASE; ORAL Discontinued No None


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