Visitor Monitoring Drug History: OPANA
 
Drugs Directory of False Positives DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
 
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Label and Approval History

Drug Name: OPANA
FDA Application No: (NDA) 021611
Active Ingredient(s): OXYMORPHONE HYDROCHLORIDE
Company: ENDO PHARMS
 
Label History
 
View the label approved on August 4, 2006 for OPANA, (NDA) 021611


To see older, previously-approved labels, go to the "Approval History" section of this page. Older labels are for historical information only and should not be used for clinical purposes.
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
8/2/2006 001Labeling Revision Letter
Label 
6/22/2006 000Approval Letter
Label 
 
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