Visitor Monitoring Drug History: COLESTID
 
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: COLESTID
FDA Application No: (NDA) 017563
Active Ingredient(s): COLESTIPOL HYDROCHLORIDE
Company: PHARMACIA AND UPJOHN
 
Label History
 
Labels are not available on this site for COLESTID, (NDA) 017563
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
9/22/1995 021Labeling Revision  
1/18/1996 020Control Supplement  
3/26/1996 019Control Supplement  
4/9/1992 017Labeling Revision  
12/18/1991 016Labeling Revision  
6/1/1992 015Package Change  
6/17/1991 014Labeling Revision  
12/6/1993 013Formulation Revision  
8/6/1991 012Labeling Revision  
7/27/1990 011Labeling Revision  
4/3/1987 010Expiration Date Change  
11/24/1986 009Labeling Revision  
2/25/1985 007Control Supplement  
2/19/1982 006Labeling Revision  
2/19/1982 005Labeling Revision  
2/19/1982 004Labeling Revision  
4/17/1979 003Labeling Revision  
7/23/1979 002Package Change  
5/16/1977 001Manufacturing Change or Addition  
4/4/1977 000Approval  
 
Therapeutic Equivalents
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