Visitor Monitoring Drug History: FUDR
 
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: FUDR
FDA Application No: (NDA) 016929
Active Ingredient(s): FLOXURIDINE
Company: HOSPIRA
 
Label History
 
View the label approved on January 9, 2004 for FUDR, (NDA) 016929


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
9/20/1999 027Manufacturing Change or Addition Label 
9/15/1997 026Control Supplement  
10/19/1992 025Control Supplement  
7/12/1990 024Control Supplement  
7/30/1990 023Control Supplement  
3/20/1989 022Control Supplement  
4/12/1988 021Control Supplement  
6/1/1987 020Labeling Revision  
1/15/1987 019Labeling Revision  
1/9/1987 018Manufacturing Change or Addition  
9/23/1985 017Manufacturing Change or Addition  
4/4/1984 016Control Supplement  
5/14/1990 015Practioner Draft Labeling  
8/22/1990 014Labeling Revision  
4/7/1978 013Labeling Revision  
1/9/1978 012Control Supplement  
9/15/1977 011Control Supplement  
2/23/1977 009Control Supplement  
2/25/1976 008Control Supplement  
2/25/1976 006Control Supplement  
12/18/1970 000Approval  
 
Therapeutic Equivalents
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