Visitor Monitoring Drug History: ALBUTEROL SULFATE
 
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Label and Approval History

Drug Name: ALBUTEROL SULFATE
FDA Application No: (ANDA) 072151
Active Ingredient(s): ALBUTEROL SULFATE
Company: SANDOZ
 
Label History
 
Labels are not available on this site for ALBUTEROL SULFATE, (ANDA) 072151
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
4/19/2002 018Control Supplement  
12/13/2001 017Control Supplement  
2/7/2002 016Control Supplement  
11/30/2000 015Control Supplement  
5/5/1999 014Chemistry  
4/23/1998 013Labeling  
11/5/1997 012Chemistry  
12/7/1995 011Chemistry  
8/23/1994 010Labeling  
1/24/1994 009Chemistry  
8/23/1994 007Chemistry  
8/23/1994 006Chemistry  
8/23/1994 005Chemistry  
10/6/1993 004Labeling  
5/10/1991 003Labeling in Effect  
12/18/1990 002Labeling in Effect  
3/23/1989 000Approval  
 
Therapeutic Equivalents
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