Visitor Monitoring Drug History: PROVENTIL
 
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: PROVENTIL
FDA Application No: (NDA) 019383
Active Ingredient(s): ALBUTEROL SULFATE
Company: SCHERING
 
Label History
 
Labels are not available on this site for PROVENTIL, (NDA) 019383
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
4/9/2001 019Control Supplement  
7/15/1998 013Manufacturing Change or Addition  
9/18/1997 011New or Modified Indication  
11/6/1998 010Labeling Revision Review 
5/24/1999 009Control Supplement  
9/9/1996 008Manufacturing Change or Addition  
5/27/1993 004Control Supplement  
12/12/1997 003Control Supplement  
6/5/1992 002Control Supplement  
1/24/1989 001Manufacturing Change or Addition  
7/13/1987 000Approval  
 
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