Visitor Monitoring Drug History: KEFLET
 
Drugs Directory of False Positives DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
 
Browse by Letter: A B C D E F G H I J K L M N O P Q R S T U V W X Y Z 0-9
Label and Approval History

Drug Name: KEFLET
FDA Application No: (NDA) 050440
Active Ingredient(s): CEPHALEXIN
Company: LILLY
 
Label History
 
Labels are not available on this site for KEFLET, (NDA) 050440
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
9/17/1982 045Labeling Revision  
9/17/1982 044Labeling Revision  
9/17/1982 043New Dosage Regimen  
3/9/1982 042Control Supplement  
9/4/1981 041Labeling Revision  
2/11/1981 040Control Supplement  
12/31/1980 039Labeling Revision  
5/12/1980 038Labeling Revision  
3/19/1980 037Formulation Revision  
3/4/1980 036Control Supplement  
11/21/1979 035Labeling Revision  
5/21/1979 034Labeling Revision  
4/20/1979 033Control Supplement  
1/13/1979 031Labeling Revision  
11/7/1978 030New Dosage Regimen  
5/18/1978 029Control Supplement  
5/25/1977 028Manufacturing Change or Addition  
3/11/1977 027Control Supplement  
2/28/1977 026Labeling Revision  
11/2/1976 025Labeling Revision  
11/8/1976 024Expiration Date Change  
11/17/1975 023Labeling Revision  
10/20/1975 022Formulation Revision  
6/20/1975 021Labeling Revision  
12/27/1974 020Expiration Date Change  
7/30/1991 019Labeling Revision  
4/10/1990 018Labeling Revision  
7/16/1986 011Labeling Revision  
1/27/1987 009Control Supplement  
11/22/1985 008Labeling Revision  
9/6/1985 007Labeling Revision  
9/5/1984 006Control Supplement  
9/28/1983 005Labeling Revision  
9/28/1983 004Labeling Revision  
8/15/1983 003Manufacturing Change or Addition  
2/15/1983 002Control Supplement  
10/12/1972 000Approval  
 
Therapeutic Equivalents
©2019 Drugs That Causes a False Positive on a Drug Test