Visitor Monitoring Drug History: PATHILON
 
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: PATHILON
FDA Application No: (NDA) 009489
Active Ingredient(s): TRIDIHEXETHYL CHLORIDE
Company: LEDERLE
 
Label History
 
Labels are not available on this site for PATHILON, (NDA) 009489
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
11/7/1991 025Formulation Revision  
1/9/1990 024Labeling Revision  
3/27/1989 023Labeling Revision  
9/28/1988 022Formulation Revision  
7/16/1987 021Labeling Revision  
9/15/1954 000Approval  
 
There are no Therapeutic Equivalents
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