Visitor Monitoring Drug History: LASIX
 
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Label and Approval History

Drug Name: LASIX
FDA Application No: (NDA) 016363
Active Ingredient(s): FUROSEMIDE
Company: SANOFI AVENTIS US
 
Label History
 
Labels are not available on this site for LASIX, (NDA) 016363
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
6/24/1996 058Manufacturing Change or Addition  
8/4/1995 057Control Supplement  
3/6/1996 056Labeling Revision  
4/3/1995 055Control Supplement  
5/1/1995 054Manufacturing Change or Addition  
1/26/1995 053Labeling Revision  
7/9/1993 052Formulation Revision  
9/2/1993 051Control Supplement  
7/9/1993 050Labeling Revision  
7/7/1993 049Manufacturing Change or Addition  
1/26/1995 048Labeling Revision  
11/13/1992 047Labeling Revision  
1/15/1992 046Labeling Revision  
9/14/1990 045Labeling Revision  
1/5/1990 044Control Supplement  
3/15/1990 043Practioner Draft Labeling  
8/10/1990 042Control Supplement  
2/25/1988 041Package Change  
10/22/1987 040Manufacturing Change or Addition  
1/22/1986 039Expiration Date Change  
10/1/1984 038Control Supplement  
6/7/1984 037Manufacturing Change or Addition  
10/22/1982 036Package Change  
6/14/1983 035Labeling Revision  
6/4/1982 034Control Supplement  
6/2/1986 033Practioner Draft Labeling  
8/28/1981 032Practioner Draft Labeling  
2/5/1981 030General Efficacy (MarkIV)  
3/5/1981 029Labeling Revision  
6/25/1979 028Control Supplement  
7/2/1979 027Labeling Revision  
11/12/1979 026Control Supplement  
2/22/1979 025Labeling Revision  
2/22/1979 024Labeling Revision  
4/14/1978 023Labeling Revision  
4/14/1978 022Labeling Revision  
8/21/1979 020Control Supplement  
6/29/1976 018Labeling Revision  
9/29/1975 017Control Supplement  
3/20/1975 002Other Amendment  
3/20/1968 000Approval  
 
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