Visitor Monitoring Drug History: CHLORDIAZEPOXIDE HYDROCHLORIDE
 
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Label and Approval History

Drug Name: CHLORDIAZEPOXIDE HYDROCHLORIDE
FDA Application No: (ANDA) 083116
Active Ingredient(s): CHLORDIAZEPOXIDE HYDROCHLORIDE
Company: BARR
 
Label History
 
Labels are not available on this site for CHLORDIAZEPOXIDE HYDROCHLORIDE, (ANDA) 083116
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
12/4/2001 104Control Supplement  
5/31/2000 103Facility Addition  
11/2/2001 102Control Supplement  
12/21/1999 101Facility Addition  
5/13/1999 100Chemistry  
5/20/1999 099Chemistry  
11/16/1998 098Chemistry  
12/1/1998 097Chemistry  
4/16/1997 096Chemistry  
12/23/1994 095Chemistry  
8/2/1993 094Labeling in Effect  
4/3/1992 093Chemistry  
4/3/1992 091Chemistry  
5/1/1989 090Labeling  
7/17/1987 086Chemistry  
11/19/1985 082Chemistry  
11/19/1985 081Chemistry  
11/19/1985 080Chemistry  
11/19/1985 079Chemistry  
11/19/1985 078Chemistry  
3/29/1982 068Chemistry  
5/13/1982 059Chemistry  
6/10/1976 000Approval  
 
Therapeutic Equivalents
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