Visitor Monitoring Drug History: NEBCIN
 
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: NEBCIN
FDA Application No: (NDA) 050519
Active Ingredient(s): TOBRAMYCIN SULFATE
Company: LILLY
 
Label History
 
Labels are not available on this site for NEBCIN, (NDA) 050519
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
4/2/2003 024Labeling Revision Letter 
10/1/1997 022Patient Population Altered  
1/2/1997 021Control Supplement  
12/20/1995 020Manufacturing Change or Addition  
3/19/1997 019Labeling Revision  
4/1/1993 018Labeling Revision  
7/20/1982 017Control Supplement  
6/9/1982 016Labeling Revision  
10/2/1981 015Labeling Revision  
8/28/1981 014Control Supplement  
5/29/1981 013Labeling Revision  
3/6/1981 012Labeling Revision  
6/5/1981 011Expiration Date Change  
9/30/1981 010Labeling Revision  
9/18/1980 009Control Supplement  
8/6/1992 008Labeling Revision  
10/28/1991 006Labeling Revision  
11/4/1985 005Labeling Revision  
5/20/1985 004Package Change  
10/4/1984 003Manufacturing Change or Addition  
8/4/1983 002Control Supplement  
1/18/1983 001Labeling Revision  
6/11/1979 000Approval  
 
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