Visitor Monitoring Drug History: ALBUTEROL SULFATE
 
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Label and Approval History

Drug Name: ALBUTEROL SULFATE
FDA Application No: (ANDA) 073533
Active Ingredient(s): ALBUTEROL SULFATE
Company: ACTAVIS MID ATLANTIC
 
Label History
 
Labels are not available on this site for ALBUTEROL SULFATE, (ANDA) 073533
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
1/25/2002 016Facility Addition  
4/3/2001 014Microbiology  
8/17/2000 013Labeling  
8/17/2000 012Expiration Date Change  
8/17/2000 011Packaging Addition  
3/21/2000 010Control Supplement  
7/20/1999 009Chemistry  
4/23/1998 008Labeling  
7/16/1999 007Chemistry  
7/16/1999 006Chemistry  
7/16/1999 005Chemistry  
7/16/1999 004Chemistry  
7/16/1999 003Chemistry  
7/16/1999 002Chemistry  
1/28/1997 001Chemistry  
9/26/1995 000Approval  
 
Therapeutic Equivalents
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