Visitor Monitoring Drug History: CECLOR
 
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: CECLOR
FDA Application No: (NDA) 050522
Active Ingredient(s): CEFACLOR
Company: LILLY
 
Label History
 
View the label approved on April 5, 2004 for CECLOR, (NDA) 050522


To see older, previously-approved labels, go to the "Approval History" section of this page. Older labels are for historical information only and should not be used for clinical purposes.
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
3/17/2004 027Labeling Revision Letter
Label 
3/3/2003 024Labeling Revision Letter 
10/12/2001 023Labeling Revision  
4/27/2000 022Control Supplement  
3/13/2000 021Control Supplement  
3/16/2000 020Manufacturing Change or Addition  
9/18/1998 019Labeling Revision  
2/2/1998 018Labeling Revision Review 
3/5/1996 015Labeling Revision  
9/30/1996 014Labeling Revision  
3/6/1996 013Labeling Revision  
5/28/1993 012Labeling Revision  
4/13/1995 011Labeling Revision  
12/8/1992 010Control Supplement  
5/1/1996 008Labeling Revision  
5/1/1996 007Labeling Revision  
7/21/1988 006Labeling Revision  
8/28/1986 002Labeling Revision  
7/14/1986 001Labeling Revision  
4/4/1979 000Approval  
 
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