Visitor Monitoring Drug History: ALBUTEROL SULFATE
 
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Label and Approval History

Drug Name: ALBUTEROL SULFATE
FDA Application No: (ANDA) 074880
Active Ingredient(s): ALBUTEROL SULFATE
Company: NEPHRON
 
Label History
 
Labels are not available on this site for ALBUTEROL SULFATE, (ANDA) 074880
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
6/6/2001 011Manufacturing Revision  
6/6/2001 010Control Supplement  
8/17/2000 008Packaging Addition  
8/17/2000 007Labeling  
10/29/1999 005Facility Addition  
7/21/1999 003Chemistry  
10/26/1998 002Labeling  
11/20/1997 001Labeling  
9/17/1997 000Approval  
 
Therapeutic Equivalents
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