Visitor Monitoring Drug History: NALTREXONE HYDROCHLORIDE
 
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: NALTREXONE HYDROCHLORIDE
FDA Application No: (ANDA) 075434
Active Ingredient(s): NALTREXONE HYDROCHLORIDE
Company: SANDOZ
 
Label History
 
View the label approved on June 9, 2004 for NALTREXONE HYDROCHLORIDE, (ANDA) 075434


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
8/11/2000 001Facility Addition  
3/8/2000 000Approval Letter
Label
Review 
 
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