Visitor Monitoring Drug History: ALBUTEROL SULFATE
 
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Label and Approval History

Drug Name: ALBUTEROL SULFATE
FDA Application No: (ANDA) 075262
Active Ingredient(s): ALBUTEROL SULFATE
Company: ACTAVIS MID ATLANTIC
 
Label History
 
Labels are not available on this site for ALBUTEROL SULFATE, (ANDA) 075262
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
12/13/2001 001Facility Addition  
3/30/1999 000Approval Letter 
 
Therapeutic Equivalents
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