Visitor Monitoring Drug History: CHLORDIAZEPOXIDE HYDROCHLORIDE
 
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Label and Approval History

Drug Name: CHLORDIAZEPOXIDE HYDROCHLORIDE
FDA Application No: (ANDA) 084769
Active Ingredient(s): CHLORDIAZEPOXIDE HYDROCHLORIDE
Company: BARR
 
Label History
 
Labels are not available on this site for CHLORDIAZEPOXIDE HYDROCHLORIDE, (ANDA) 084769
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
12/4/2001 088Control Supplement  
7/13/2000 087Facility Addition  
11/2/2001 086Control Supplement  
12/21/1999 085Facility Addition  
5/13/1999 084Chemistry  
5/20/1999 083Chemistry  
11/16/1998 082Chemistry  
12/1/1998 081Chemistry  
4/16/1997 080Chemistry  
8/28/1996 079Chemistry  
12/23/1994 078Chemistry  
8/2/1993 077Labeling in Effect  
4/3/1992 076Chemistry  
4/3/1992 074Chemistry  
5/10/1989 073Labeling  
7/17/1987 071Chemistry  
7/17/1987 070Chemistry  
3/20/1987 069Chemistry  
7/31/1986 066Chemistry  
7/31/1986 062Chemistry  
7/31/1986 061Chemistry  
7/31/1986 060Chemistry  
3/3/1982 047Chemistry  
10/30/1980 037Chemistry  
1/13/1977 007Chemistry  
6/10/1976 000Approval  
 
Therapeutic Equivalents
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