Visitor Monitoring Drug History: QUINAGLUTE
 
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Label and Approval History

Drug Name: QUINAGLUTE
FDA Application No: (NDA) 016647
Active Ingredient(s): QUINIDINE GLUCONATE
Company: BAYER HLTHC
 
Label History
 
Labels are not available on this site for QUINAGLUTE, (NDA) 016647
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
4/26/2001 039Package Change  
11/14/2000 038Expiration Date Change  
3/31/1999 037Manufacturing Change or Addition  
6/24/2000 036Labeling Revision  
7/1/1998 035Labeling Revision  
11/16/1995 034Manufacturing Change or Addition  
8/17/1995 033Labeling Revision  
6/30/1987 031Control Supplement  
4/14/1987 030Control Supplement  
4/14/1989 029Labeling Revision  
7/14/1986 028Package Change  
7/30/1985 027Control Supplement  
4/2/1984 025Control Supplement  
1/23/1984 024Expiration Date Change  
1/23/1984 023Expiration Date Change  
1/23/1984 022Expiration Date Change  
4/7/1982 021Expiration Date Change  
4/7/1981 020Manufacturing Change or Addition  
4/7/1981 019Control Supplement  
2/25/1981 017Control Supplement  
8/27/1980 015Package Change  
8/27/1979 014Control Supplement  
8/27/1979 013Control Supplement  
7/24/1979 012Control Supplement  
9/25/1979 011Control Supplement  
6/2/1978 010Control Supplement  
7/25/1978 009Control Supplement  
10/6/1977 008Manufacturing Change or Addition  
10/6/1977 006Control Supplement  
10/6/1977 005Labeling Revision  
10/6/1977 004Other Amendment  
12/8/1969 000Approval  
 
Therapeutic Equivalents
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