Visitor Monitoring Drug Details: ONDANSETRON
 
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Drug Details

Drug Name: ONDANSETRON
FDA Application No: (ANDA) 077729
Active Ingredient(s): ONDANSETRON HYDROCHLORIDE
Company: TARO PHARM INDS
Original Approval or Tentative Approval Date: April 14, 2006
 
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
ONDANSETRON ONDANSETRON HYDROCHLORIDE4MGTABLET; ORAL Tentative Approval No None
ONDANSETRON ONDANSETRON HYDROCHLORIDE8MGTABLET; ORAL Tentative Approval No None
ONDANSETRON ONDANSETRON HYDROCHLORIDE24MGTABLET; ORAL Tentative Approval No None


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