Visitor Monitoring Drug Details: ZONALON
 
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Drug Details

Drug Name: ZONALON
FDA Application No: (NDA) 020126
Active Ingredient(s): DOXEPIN HYDROCHLORIDE
Company: BRADLEY PHARMS
Original Approval or Tentative Approval Date: April 1, 1994
Chemical Type: 3 New dosage form
Review Classification: S Standard review drug
 
 
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
ZONALON DOXEPIN HYDROCHLORIDE5%CREAM; TOPICAL Prescription Yes None


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