Visitor Monitoring Drug History: TAGAMET
 
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: TAGAMET
FDA Application No: (NDA) 017924
Active Ingredient(s): CIMETIDINE HYDROCHLORIDE
Company: GLAXOSMITHKLINE
 
Label History
 
Labels are not available on this site for TAGAMET, (NDA) 017924
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
4/15/1997 059Control Supplement  
2/22/1995 058Labeling Revision  
11/10/1993 057Manufacturing Change or Addition  
6/8/1993 056Manufacturing Change or Addition  
7/16/1992 054Control Supplement  
1/7/1992 053Labeling Revision  
8/27/1992 052Control Supplement  
11/13/1991 050Labeling Revision  
11/13/1989 049Labeling Revision  
5/30/1990 047Control Supplement  
3/7/1991 046Labeling Revision  
6/26/1989 045Labeling Revision  
6/26/1989 044Labeling Revision  
6/15/1988 042Labeling Revision  
5/20/1988 041Labeling Revision  
3/31/1988 040New Dosage Regimen  
4/23/1986 038Labeling Revision  
1/13/1986 037Labeling Revision  
5/15/1985 036Labeling Revision  
4/18/1985 035Labeling Revision  
2/7/1985 034Labeling Revision  
4/29/1986 033New Dosage Regimen  
6/14/1984 032Labeling Revision  
7/19/1984 031Labeling Revision  
12/5/1984 030Package Change  
3/5/1984 029Labeling Revision  
7/19/1984 027Labeling Revision  
2/28/1983 025Labeling Revision  
1/31/1983 024General Efficacy (MarkIV)  
3/11/1983 023Manufacturing Change or Addition  
8/25/1982 022General Efficacy (MarkIV)  
1/22/1982 019Labeling Revision  
12/30/1982 018Labeling Revision  
11/2/1981 017Labeling Revision  
7/13/1981 016Labeling Revision  
6/12/1981 014Formulation Revision  
1/22/1981 013Labeling Revision  
1/22/1981 012Labeling Revision  
12/30/1982 011General Efficacy (MarkIV)  
7/8/1980 010Labeling Revision  
1/8/1980 008Control Supplement  
8/16/1977 000Approval  
 
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