Visitor Monitoring Drug History: ACCUNEB
 
Drugs Directory of False Positives DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
 
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Label and Approval History

Drug Name: ACCUNEB
FDA Application No: (NDA) 020949
Active Ingredient(s): ALBUTEROL SULFATE
Company: DEY
 
Label History
 
Labels are not available on this site for ACCUNEB, (NDA) 020949
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
6/2/2006 011Labeling Revision Letter
Patient Information Sheet 
11/13/2002 009Control Supplement  
8/6/2002 007Manufacturing Change or Addition  
2/20/2002 005Control Supplement  
2/20/2002 004Control Supplement  
1/22/2002 002Control Supplement  
1/22/2002 001Control Supplement  
4/30/2001 000Approval Review 
 
Therapeutic Equivalents
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