Visitor Monitoring Drug History: CHLORDIAZEPOXIDE HYDROCHLORIDE
 
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Label and Approval History

Drug Name: CHLORDIAZEPOXIDE HYDROCHLORIDE
FDA Application No: (ANDA) 084679
Active Ingredient(s): CHLORDIAZEPOXIDE HYDROCHLORIDE
Company: SANDOZ
 
Label History
 
Labels are not available on this site for CHLORDIAZEPOXIDE HYDROCHLORIDE, (ANDA) 084679
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
2/3/1995 081Labeling  
4/7/1989 079Labeling  
7/23/1987 077Chemistry  
7/23/1987 076Chemistry  
7/23/1987 075Chemistry  
1/8/1985 073Chemistry  
5/25/1984 071Chemistry  
1/13/1984 070Chemistry  
1/13/1984 069Chemistry  
6/20/1983 068Chemistry  
7/22/1982 063Chemistry  
7/1/1982 062Chemistry  
3/15/1982 060Chemistry  
3/15/1982 059Chemistry  
3/15/1982 058Chemistry  
3/15/1982 057Chemistry  
3/15/1982 056Chemistry  
6/15/1976 000Approval  
 
Therapeutic Equivalents
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