Visitor Monitoring Drug Details: ULTRAM ER
 
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Drug Details

Drug Name: ULTRAM ER
FDA Application No: (NDA) 021692
Active Ingredient(s): TRAMADOL HYDROCHLORIDE
Company: BIOVAIL LABS INTL
Original Approval or Tentative Approval Date: September 8, 2005
Chemical Type: 5 New manufacturer
Review Classification: S Standard review drug
 
There are no Therapeutic Equivalents Label Information
Approval History, Letters, Reviews and Related Documents
 
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Drug NameSort imageActive IngredientsStrengthDosage Form/RouteMarketing StatusRLDTE Code
ULTRAM ER TRAMADOL HYDROCHLORIDE100MGTABLET, EXTENDED RELEASE; ORAL Prescription Yes None
ULTRAM ER TRAMADOL HYDROCHLORIDE200MGTABLET, EXTENDED RELEASE; ORAL Prescription No None
ULTRAM ER TRAMADOL HYDROCHLORIDE300MGTABLET, EXTENDED RELEASE; ORAL Prescription No None


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