Visitor Monitoring Drug History: KEFLIN
 
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: KEFLIN
FDA Application No: (NDA) 050482
Active Ingredient(s): CEPHALOTHIN SODIUM
Company: LILLY
 
Label History
 
Labels are not available on this site for KEFLIN, (NDA) 050482
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
1/19/1993 027Labeling Revision  
3/20/1987 024Control Supplement  
10/30/1986 021Control Supplement  
12/17/1985 019Labeling Revision  
11/25/1985 018New or Modified Indication  
6/7/1985 017Control Supplement  
5/8/1985 016Control Supplement  
9/7/1984 015Control Supplement  
3/8/1984 014Control Supplement  
12/5/1983 013Labeling Revision  
10/5/1983 012Control Supplement  
8/24/1983 011Labeling Revision  
8/5/1983 010Labeling Revision  
8/5/1983 009Labeling Revision  
6/21/1983 008Labeling Revision  
6/20/1983 007Labeling Revision  
3/18/1983 006Labeling Revision  
3/8/1983 005Labeling Revision  
2/17/1983 004Control Supplement  
2/1/1983 003Control Supplement  
1/13/1983 002Control Supplement  
11/17/1982 001Control Supplement  
12/18/1974 000Approval  
 
Therapeutic Equivalents
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