Visitor Monitoring Drug History: FURADANTIN
 
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Label and Approval History

Drug Name: FURADANTIN
FDA Application No: (NDA) 008693
Active Ingredient(s): NITROFURANTOIN
Company: PROCTER AND GAMBLE
 
Label History
 
Labels are not available on this site for FURADANTIN, (NDA) 008693
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
7/16/1997 030Labeling Revision  
3/27/1997 029Labeling Revision  
2/17/1998 028Labeling Revision  
8/9/1993 027Control Supplement  
2/17/1998 026Labeling Revision  
5/13/1988 025Labeling Revision Review 
7/14/1983 021Manufacturing Change or Addition  
5/18/1993 020New or Modified Indication  
11/18/1982 019Labeling Revision  
6/29/1979 017Manufacturing Change or Addition  
12/17/1979 016Labeling Revision  
3/16/1979 015Package Change  
5/11/1976 011Manufacturing Change or Addition  
6/30/1976 010Manufacturing Change or Addition  
2/6/1953 000Approval  
 
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