Visitor Monitoring Drug History: HALFAN
 
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: HALFAN
FDA Application No: (NDA) 020250
Active Ingredient(s): HALOFANTRINE HYDROCHLORIDE
Company: GLAXOSMITHKLINE
 
Label History
 
View the label approved on August 1, 2002 for HALFAN, (NDA) 020250


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
8/1/2002 008Labeling Revision Letter
Label 
8/1/2002 007Labeling Revision Letter
Label 
8/6/1997 006Labeling Revision  
9/23/1993 005Package Change  
2/12/1993 003Labeling Revision  
8/6/1997 002Labeling Revision  
12/2/1992 001Manufacturing Change or Addition  
7/24/1992 000Approval  
 
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