Visitor Monitoring Drug Details: SONATA
 
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Drug Details

Drug Name: SONATA
FDA Application No: (NDA) 020859
Active Ingredient(s): ZALEPLON
Company: KING PHARMS
Original Approval or Tentative Approval Date: August 13, 1999
Chemical Type: 1 New molecular entity (NME)
Review Classification: S Standard review drug
 
Therapeutic Equivalents Label Information
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
SONATA ZALEPLON5MGCAPSULE; ORAL Prescription No None
SONATA ZALEPLON10MGCAPSULE; ORAL Prescription Yes None


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