Visitor Monitoring Drug History: LASIX
 
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Label and Approval History

Drug Name: LASIX
FDA Application No: (NDA) 016273
Active Ingredient(s): FUROSEMIDE
Company: SANOFI AVENTIS US
 
Label History
 
Labels are not available on this site for LASIX, (NDA) 016273
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
2/8/2006 057Labeling Revision Letter 
1/14/1999 056Package Change  
10/8/1998 055Package Change  
12/4/1997 054Manufacturing Change or Addition  
6/24/1996 053Manufacturing Change or Addition  
5/1/1995 052Manufacturing Change or Addition  
1/26/1995 051Labeling Revision  
11/13/1992 050Labeling Revision  
4/6/1992 049Package Change  
6/1/1992 048Package Change  
10/23/1991 047Labeling Revision  
3/15/1990 046Practioner Draft Labeling  
3/8/1991 045Control Supplement  
2/9/1987 044Manufacturing Change or Addition  
9/14/1983 043Expiration Date Change  
8/2/1983 042Manufacturing Change or Addition  
3/15/1983 040Package Change  
8/2/1982 039Package Change  
6/2/1986 038Practioner Draft Labeling  
2/4/1981 036Manufacturing Change or Addition  
3/27/1981 035Labeling Revision  
7/2/1979 034Labeling Revision  
2/5/1980 033Package Change  
4/24/1978 031Labeling Revision  
4/24/1978 030Labeling Revision  
4/24/1978 029Control Supplement  
4/24/1978 028Labeling Revision  
2/9/1977 027Package Change  
1/10/1977 026Expiration Date Change  
7/21/1976 023Labeling Revision  
3/20/1975 007Other Amendment  
7/1/1966 000Approval  
 
Therapeutic Equivalents
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