Visitor Monitoring Drug History: CATAPRES
 
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: CATAPRES
FDA Application No: (NDA) 017407
Active Ingredient(s): CLONIDINE HYDROCHLORIDE
Company: BOEHRINGER INGELHEIM
 
Label History
 
Labels are not available on this site for CATAPRES, (NDA) 017407
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
4/13/1999 031Manufacturing Change or Addition  
4/30/1998 030Control Supplement  
11/3/1997 029Control Supplement  
8/2/1996 028Labeling Revision  
8/2/1996 027Labeling Revision  
6/20/1988 026Labeling Revision  
3/26/1987 025Labeling Revision  
9/2/1987 024Manufacturing Change or Addition  
4/11/1986 023Labeling Revision  
10/2/1985 022Labeling Revision  
3/6/1985 021Control Supplement  
4/6/1984 020Formulation Revision  
9/8/1987 019Practioner Draft Labeling  
11/3/1982 018Manufacturing Change or Addition  
8/5/1981 017Package Change  
4/6/1981 016Package Change  
2/20/1981 015Package Change  
2/20/1981 014Package Change  
9/12/1980 013Package Change  
9/16/1980 012Expiration Date Change  
2/26/1980 011Package Change  
12/10/1980 010Package Change  
11/27/1978 009Package Change  
9/20/1979 008General Efficacy (MarkIV)  
2/5/1981 006Package Change  
12/10/1976 005Package Change  
1/17/1977 004Package Change  
10/27/1976 003Formulation Revision  
7/26/1976 002Package Change  
6/8/1976 001Package Change  
9/3/1974 000Approval  
 
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