Visitor Monitoring Drug History: KEFTAB
 
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: KEFTAB
FDA Application No: (NDA) 050614
Active Ingredient(s): CEPHALEXIN HYDROCHLORIDE
Company: LILLY
 
Label History
 
Labels are not available on this site for KEFTAB, (NDA) 050614
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
6/18/2001 021Manufacturing Change or Addition  
12/15/2000 020Manufacturing Change or Addition  
7/29/1999 019Labeling Revision  
7/29/1999 018Labeling Revision  
2/19/1998 017Package Change  
7/29/1999 016Labeling Revision  
9/2/1993 015Manufacturing Change or Addition  
5/16/1988 014Control Supplement  
6/28/1993 013Labeling Revision  
10/25/1991 011Control Supplement  
9/6/1991 010Labeling Revision  
11/28/1990 009Control Supplement  
3/8/1991 008Chemistry Generic  
10/29/1987 000Approval  
 
There are no Therapeutic Equivalents
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