Visitor Monitoring Drug Details: MEBENDAZOLE
 
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Drug Details

Drug Name: MEBENDAZOLE
FDA Application No: (ANDA) 073580
Active Ingredient(s): MEBENDAZOLE
Company: TEVA PHARMS
Original Approval or Tentative Approval Date: January 4, 1995
 
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
MEBENDAZOLE MEBENDAZOLE100MGTABLET, CHEWABLE; ORAL Prescription Yes None


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