Visitor Monitoring Drug Details: ONDANSETRON
 
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Drug Details

Drug Name: ONDANSETRON
FDA Application No: (ANDA) 077406
Active Ingredient(s): ONDANSETRON
Company: KALI LABS
Original Approval or Tentative Approval Date: December 26, 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 ONDANSETRON16MGTABLET, ORALLY DISINTEGRATING; ORAL Prescription No None
ONDANSETRON ONDANSETRON24MGTABLET, ORALLY DISINTEGRATING; ORAL Prescription No None


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