Visitor Monitoring Drug History: QUELICIN
 
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Label and Approval History

Drug Name: QUELICIN
FDA Application No: (NDA) 008845
Active Ingredient(s): SUCCINYLCHOLINE CHLORIDE
Company: HOSPIRA
 
Label History
 
Labels are not available on this site for QUELICIN, (NDA) 008845
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
12/17/2002 055Expiration Date Change  
11/17/2000 054Control Supplement  
6/30/2000 053Labeling Revision  
1/29/1999 052Labeling Revision  
5/26/1998 050Manufacturing Change or Addition  
1/29/1999 049Labeling Revision  
10/27/1997 048Package Change  
11/28/1994 047Labeling Revision  
5/3/1989 046Labeling Revision  
5/3/1989 045Control Supplement  
5/27/1988 044Package Change  
3/16/1987 043Package Change  
9/1/1987 042Labeling Revision  
9/1/1987 041Labeling Revision  
9/1/1987 040Package Change  
6/27/1984 037Control Supplement  
5/5/1982 034Labeling Revision  
10/23/1981 033Labeling Revision  
11/10/1981 032Control Supplement  
8/6/1981 031Control Supplement  
5/16/1981 030Package Change  
9/3/1980 029Control Supplement  
3/16/1982 028Labeling Revision  
9/3/1980 027Control Supplement  
9/3/1980 026Control Supplement  
2/10/1981 025Control Supplement  
12/3/1980 024Package Change  
12/11/1979 023Control Supplement  
8/22/1978 022Control Supplement  
4/18/1978 021Control Supplement  
6/20/1977 020Control Supplement  
9/6/1977 019Labeling Revision  
9/6/1977 018Control Supplement  
12/14/1976 017Labeling Revision  
12/14/1976 016Control Supplement  
7/20/1976 015Labeling Revision  
12/14/1976 014Expiration Date Change  
5/6/1976 013Labeling Revision  
5/6/1976 012Labeling Revision  
6/22/1976 011Control Supplement  
5/1/1953 000Approval  
 
Therapeutic Equivalents
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