Visitor Monitoring Drug Details: ZALEPLON
 
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Drug Details

Drug Name: ZALEPLON
FDA Application No: (ANDA) 077238
Active Ingredient(s): ZALEPLON
Company: GENPHARM
Original Approval or Tentative Approval Date: July 26, 2006
 
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
ZALEPLON ZALEPLON5MGCAPSULE; ORAL Tentative Approval No None
ZALEPLON ZALEPLON10MGCAPSULE; ORAL Tentative Approval No None


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