Visitor Monitoring Drug History: CHLORDIAZEPOXIDE HYDROCHLORIDE
 
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Label and Approval History

Drug Name: CHLORDIAZEPOXIDE HYDROCHLORIDE
FDA Application No: (ANDA) 084768
Active Ingredient(s): CHLORDIAZEPOXIDE HYDROCHLORIDE
Company: BARR
 
Label History
 
Labels are not available on this site for CHLORDIAZEPOXIDE HYDROCHLORIDE, (ANDA) 084768
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
12/4/2001 085Control Supplement  
6/23/2000 084Manufacturing Revision  
6/23/2000 083Facility Addition  
12/21/1999 081Facility Addition  
5/13/1999 080Chemistry  
5/20/1999 079Chemistry  
11/16/1998 078Chemistry  
12/1/1998 077Chemistry  
4/16/1997 076Chemistry  
12/23/1994 075Chemistry  
8/2/1993 074Labeling in Effect  
4/3/1992 073Chemistry  
4/3/1992 071Chemistry  
5/1/1992 070Chemistry  
5/10/1989 069Labeling  
7/17/1987 067Chemistry  
7/17/1987 066Chemistry  
3/20/1987 065Chemistry  
11/12/1985 060Chemistry  
11/12/1985 059Chemistry  
11/12/1985 058Chemistry  
11/12/1985 057Chemistry  
6/7/1982 039Chemistry  
6/10/1976 000Approval  
 
Therapeutic Equivalents
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