Visitor Monitoring Drug History: KLONOPIN
 
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: KLONOPIN
FDA Application No: (NDA) 017533
Active Ingredient(s): CLONAZEPAM
Company: ROCHE
 
Label History
 
Labels are not available on this site for KLONOPIN, (NDA) 017533
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
3/15/2002 039Expiration Date Change  
3/11/2002 038Expiration Date Change  
1/29/2002 037Labeling Revision Letter
Review 
11/7/2001 036Package Change  
9/10/2001 035Control Supplement  
1/22/2001 034Manufacturing Change or Addition  
3/28/2000 033Control Supplement  
10/18/1999 032Manufacturing Change or Addition  
4/11/2001 031Labeling Revision Letter
Review 
12/30/1997 030Package Change  
9/19/1997 029Package Change  
3/7/1997 028Expiration Date Change  
11/20/1996 027Manufacturing Change or Addition  
10/17/1996 026Manufacturing Change or Addition  
8/30/1996 025Manufacturing Change or Addition  
6/18/1996 024Control Supplement  
4/9/1997 023New or Modified Indication  
7/1/1994 022Control Supplement  
6/3/1993 021Control Supplement  
6/3/1993 020Control Supplement  
4/30/1993 019Labeling Revision  
5/28/1993 018Manufacturing Change or Addition  
4/30/1993 017Labeling Revision  
7/19/1990 016Labeling Revision  
7/19/1990 015Expiration Date Change  
5/1/1987 014Control Supplement  
12/13/1985 013Labeling Revision  
12/11/1984 012Control Supplement  
12/19/1983 010Package Change  
1/13/1981 009Control Supplement  
6/13/1980 007Package Change  
2/24/1981 006Manufacturing Change or Addition  
9/19/1979 005Control Supplement  
3/23/1979 004Package Change  
8/30/1978 003Labeling Revision  
6/30/1975 002Labeling Revision  
9/26/1975 001Control Supplement  
6/4/1975 000Approval  
 
Therapeutic Equivalents
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