Visitor Monitoring Drug History: GLUCAGON
 
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Label and Approval History

Drug Name: GLUCAGON
FDA Application No: (NDA) 012122
Active Ingredient(s): GLUCAGON HYDROCHLORIDE
Company: LILLY
 
Label History
 
Labels are not available on this site for GLUCAGON, (NDA) 012122
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
6/26/1998 043Control Supplement  
9/23/1997 042Manufacturing Change or Addition  
1/8/1998 041Control Supplement  
4/18/1997 040Labeling Revision  
5/12/1997 039Labeling Revision  
11/7/1996 038Control Supplement  
12/13/1996 037Control Supplement  
12/15/1995 036Labeling Revision  
4/19/1996 035Manufacturing Change or Addition  
4/28/1993 034Labeling Revision  
11/19/1991 033Control Supplement  
10/1/1990 032Labeling Revision  
10/11/1990 031Labeling Revision  
10/4/1990 030Labeling Revision  
12/2/1988 029Labeling Revision  
9/30/1988 028Package Change  
1/5/1988 027Labeling Revision  
4/3/1991 026Manufacturing Change or Addition  
9/30/1986 025Labeling Revision  
10/17/1985 022Control Supplement  
10/17/1985 022Labeling Revision  
12/13/1984 019Labeling Revision  
8/9/1984 018Labeling Revision  
8/2/1984 017Control Supplement  
7/21/1983 016Labeling Revision  
10/9/1981 015Manufacturing Change or Addition  
6/15/1981 014General Efficacy (MarkIV)  
2/21/1980 013General Efficacy (MarkIV)  
11/27/1979 012General Efficacy (MarkIV)  
12/31/1975 010Control Supplement  
1/27/1975 009Control Supplement  
5/20/1975 008Control Supplement  
11/14/1960 000Approval  
 
Therapeutic Equivalents
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