Visitor Monitoring Drug History: NEGGRAM
 
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: NEGGRAM
FDA Application No: (NDA) 014214
Active Ingredient(s): NALIDIXIC ACID
Company: SANOFI AVENTIS US
 
Label History
 
View the label approved on May 29, 2007 for NEGGRAM, (NDA) 014214


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
5/24/2007 057Labeling Revision Letter
Label 
9/7/2004 056Labeling Revision Letter
Label 
9/7/2004 055Labeling Revision Letter
Label 
9/7/2004 053Labeling Revision Letter
Label 
9/20/2002 052Manufacturing Change or Addition  
11/23/1999 051Labeling Revision Review 
11/23/1999 050Labeling Revision Review 
10/3/1995 049Control Supplement  
6/24/1991 048Control Supplement  
9/17/1990 047Manufacturing Change or Addition  
10/5/1990 046Manufacturing Change or Addition  
7/20/1990 045Control Supplement  
2/7/1995 044Labeling Revision  
3/21/1986 043Package Change  
4/28/1986 042Labeling Revision  
8/17/1983 040Control Supplement  
8/18/1981 038Package Change  
6/4/1981 037Package Change  
6/4/1981 036Package Change  
8/18/1981 035Package Change  
12/12/1980 034Labeling Revision  
4/9/1980 033Package Change  
2/13/1979 032Control Supplement  
7/11/1978 031Manufacturing Change or Addition  
2/23/1981 030Labeling Revision  
5/3/1978 029Labeling Revision  
6/29/1977 026Control Supplement  
3/31/1976 024Labeling Revision  
4/8/1976 023Control Supplement  
9/8/1975 022Control Supplement  
7/18/1975 021Control Supplement  
2/23/1977 020Supplement  
2/26/1975 014Supplement  
3/6/1964 000Approval  
 
Therapeutic Equivalents
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