Visitor Monitoring Drug History: CHLORDIAZEPOXIDE HYDROCHLORIDE
 
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Label and Approval History

Drug Name: CHLORDIAZEPOXIDE HYDROCHLORIDE
FDA Application No: (ANDA) 084041
Active Ingredient(s): CHLORDIAZEPOXIDE HYDROCHLORIDE
Company: SANDOZ
 
Label History
 
Labels are not available on this site for CHLORDIAZEPOXIDE HYDROCHLORIDE, (ANDA) 084041
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
2/3/1995 094Labeling  
11/3/1989 092Labeling  
5/1/1989 091Labeling  
1/8/1985 089Chemistry  
5/25/1984 086Chemistry  
1/13/1984 085Chemistry  
1/13/1984 084Chemistry  
6/21/1983 082Chemistry  
8/17/1982 079Chemistry  
8/17/1982 078Chemistry  
6/28/1982 077Chemistry  
5/27/1982 074Chemistry  
3/15/1982 073Chemistry  
3/15/1982 071Chemistry  
3/15/1982 070Chemistry  
3/15/1982 069Chemistry  
3/15/1982 068Chemistry  
6/15/1976 000Approval  
 
Therapeutic Equivalents
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