Visitor Monitoring Drug Details: LEVITRA
 
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Drug Details

Drug Name: LEVITRA
FDA Application No: (NDA) 021400
Active Ingredient(s): VARDENAFIL HYDROCHLORIDE
Company: BAYER PHARMS
Original Approval or Tentative Approval Date: August 19, 2003
Chemical Type: 1 New molecular entity (NME)
Review Classification: S Standard review drug
 
There are no 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
LEVITRA VARDENAFIL HYDROCHLORIDE5MGTABLET; ORAL Prescription No None
LEVITRA VARDENAFIL HYDROCHLORIDE10MGTABLET; ORAL Prescription No None
LEVITRA VARDENAFIL HYDROCHLORIDE2.5MGTABLET; ORAL Prescription No None
LEVITRA VARDENAFIL HYDROCHLORIDE20MGTABLET; ORAL Prescription Yes None


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