Visitor Monitoring Drug History: LASIX
 
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Label and Approval History

Drug Name: LASIX
FDA Application No: (NDA) 017688
Active Ingredient(s): FUROSEMIDE
Company: SANOFI AVENTIS US
 
Label History
 
Labels are not available on this site for LASIX, (NDA) 017688
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
6/24/1996 022Manufacturing Change or Addition  
5/1/1995 021Manufacturing Change or Addition  
12/7/1994 020Control Supplement  
8/26/1993 019Package Change  
1/26/1995 018Labeling Revision  
11/13/1992 017Labeling Revision  
6/9/1992 016Control Supplement  
11/7/1991 015Package Change  
5/23/1991 014Package Change  
10/23/1991 013Labeling Revision  
11/9/1990 012Package Change  
12/19/1991 011Control Supplement  
5/18/1990 010Package Change  
3/15/1990 009Practioner Draft Labeling  
5/29/1984 008Formulation Revision  
8/23/1982 007Control Supplement  
3/15/1990 006Practioner Draft Labeling  
1/9/1981 005Labeling Revision  
7/10/1979 004Labeling Revision  
4/14/1978 003Labeling Revision  
4/14/1978 002Labeling Revision  
4/14/1978 001Labeling Revision  
3/8/1977 000Approval  
 
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