Visitor Monitoring Drug Details: XOPENEX
 
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Drug Details

Drug Name: XOPENEX
FDA Application No: (NDA) 020837
Active Ingredient(s): LEVALBUTEROL HYDROCHLORIDE
Company: SEPRACOR
Original Approval or Tentative Approval Date: March 25, 1999
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
XOPENEX LEVALBUTEROL HYDROCHLORIDEEQ 0.021% BASESOLUTION; INHALATION Prescription Yes None
XOPENEX LEVALBUTEROL HYDROCHLORIDEEQ 0.042% BASESOLUTION; INHALATION Prescription Yes None
XOPENEX LEVALBUTEROL HYDROCHLORIDEEQ 0.0103% BASESOLUTION; INHALATION Prescription Yes None
XOPENEX LEVALBUTEROL HYDROCHLORIDEEQ 0.25% BASESOLUTION; INHALATION Prescription Yes None


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