Visitor Monitoring Drug History: FURADANTIN
 
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: FURADANTIN
FDA Application No: (NDA) 009175
Active Ingredient(s): NITROFURANTOIN
Company: SCIELE PHARMA INC
 
Label History
 
Labels are not available on this site for FURADANTIN, (NDA) 009175
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
8/25/1999 026Labeling Revision  
12/3/1998 025Package Change  
10/15/1996 024Expiration Date Change  
3/27/1997 023Labeling Revision  
4/7/1998 022Labeling Revision  
8/9/1993 021Control Supplement  
2/11/1999 020Labeling Revision  
5/13/1988 019Labeling Revision Review 
6/12/1987 016Labeling Revision  
5/18/1993 015New or Modified Indication  
11/18/1982 013Labeling Revision  
6/12/1987 012Labeling Revision  
12/17/1979 011Labeling Revision  
1/3/1978 008Manufacturing Change or Addition  
11/23/1973 006Supplement  
12/23/1953 000Approval  
 
There are no Therapeutic Equivalents
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