Visitor Monitoring Drug History: CHLORDIAZEPOXIDE HYDROCHLORIDE
 
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Label and Approval History

Drug Name: CHLORDIAZEPOXIDE HYDROCHLORIDE
FDA Application No: (ANDA) 086382
Active Ingredient(s): CHLORDIAZEPOXIDE HYDROCHLORIDE
Company: WATSON LABS
 
Label History
 
Labels are not available on this site for CHLORDIAZEPOXIDE HYDROCHLORIDE, (ANDA) 086382
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
8/3/1998 032Chemistry  
8/3/1998 031Chemistry  
9/24/1997 030Chemistry  
9/24/1997 029Chemistry  
3/26/1997 028Chemistry  
3/26/1997 027Chemistry  
8/24/1988 026SBA  
6/22/1993 024Labeling in Effect  
10/11/1988 023Chemistry  
10/11/1988 022Chemistry  
10/11/1988 021Chemistry  
7/15/1988 020Labeling  
6/10/1988 019Labeling  
7/17/1987 017Chemistry  
1/17/1986 015Chemistry  
1/17/1986 014Chemistry  
1/17/1986 013Chemistry  
1/3/1986 012Chemistry  
9/8/1978 000Approval  
 
Therapeutic Equivalents
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