Visitor Monitoring Drug History: QUESTRAN
 
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: QUESTRAN
FDA Application No: (NDA) 016640
Active Ingredient(s): CHOLESTYRAMINE
Company: BRISTOL MYERS
 
Label History
 
Labels are not available on this site for QUESTRAN, (NDA) 016640
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
8/22/1997 074Labeling Revision  
12/12/1994 071Labeling Revision  
12/12/1994 070Labeling Revision  
9/22/1995 069Labeling Revision  
9/22/1995 068Labeling Revision  
1/7/1993 067Control Supplement  
8/11/1992 066Labeling Revision  
9/22/1992 065Control Supplement  
9/10/1991 063Labeling Revision  
10/24/1991 060Labeling Revision  
5/25/1990 059Control Supplement  
3/5/1990 058Control Supplement  
3/6/1991 057Control Supplement  
2/2/1990 056Manufacturing Change or Addition  
11/28/1989 055Labeling Revision  
1/22/1990 054Formulation Revision  
2/23/1989 050Control Supplement  
12/1/1988 049Control Supplement  
10/11/1988 048Package Change  
8/26/1988 047Manufacturing Change or Addition  
8/26/1988 046Package Change  
7/14/1988 045Manufacturing Change or Addition  
7/14/1988 044Manufacturing Change or Addition  
7/14/1988 043Control Supplement  
3/2/1989 042Manufacturing Change or Addition  
6/29/1988 040Manufacturing Change or Addition  
3/25/1988 039Formulation Revision  
3/18/1988 038Control Supplement  
1/5/1988 037Formulation Revision  
2/16/1988 036Manufacturing Change or Addition  
11/19/1987 035Manufacturing Change or Addition  
11/19/1987 034Control Supplement  
12/7/1994 033Labeling Revision  
9/18/1987 030Manufacturing Change or Addition  
1/24/1986 028Control Supplement  
2/25/1986 027Labeling Revision  
9/19/1986 026Control Supplement  
3/12/1986 025Control Supplement  
9/12/1985 024Control Supplement  
11/26/1985 023Formulation Revision  
11/1/1985 022Control Supplement  
12/21/1984 021Labeling Revision  
5/11/1984 017Labeling Revision  
6/14/1984 016Control Supplement  
11/30/1983 014Labeling Revision  
6/24/1983 013Labeling Revision  
8/16/1982 012Control Supplement  
7/26/1982 011Control Supplement  
6/16/1982 010Package Change  
7/8/1981 009Labeling Revision  
2/17/1977 005Labeling Revision  
8/3/1973 000Approval  
 
Therapeutic Equivalents
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