Visitor Monitoring Drug History: BUTABARBITAL SODIUM
 
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Label and Approval History

Drug Name: BUTABARBITAL SODIUM
FDA Application No: (ANDA) 085383
Active Ingredient(s): BUTABARBITAL SODIUM
Company: MORTON GROVE
 
Label History
 
Labels are not available on this site for BUTABARBITAL SODIUM, (ANDA) 085383
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
3/6/1992 020Labeling in Effect  
12/6/1989 019Labeling  
10/10/1989 018Labeling  
8/20/1987 015Chemistry  
2/26/1987 014Chemistry  
2/26/1987 013Chemistry  
12/8/1983 008Chemistry  
7/29/1982 006Chemistry  
2/26/1979 000Approval  
 
Therapeutic Equivalents
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