Visitor Monitoring Drug History: ULTRACET
 
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: ULTRACET
FDA Application No: (NDA) 021123
Active Ingredient(s): ACETAMINOPHEN; TRAMADOL HYDROCHLORIDE
Company: ORTHO MCNEIL PHARM
 
Label History
 
View the label approved on May 3, 2004 for ULTRACET, (NDA) 021123


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
4/16/2004 001Labeling Revision Letter
Label 
8/15/2001 000Approval Letter
Label
Review 
 
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