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) 017559
Active Ingredient(s): ALBUTEROL
Company: SCHERING
 
Label History
 
Labels are not available on this site for PROVENTIL, (NDA) 017559
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
9/7/2006 040Labeling Revision Letter 
12/4/2000 032Control Supplement  
3/11/1999 027Control Supplement  
11/9/1998 023Labeling Revision Review 
9/9/1996 021Manufacturing Change or Addition  
12/15/1992 018Manufacturing Change or Addition  
1/24/1989 016Manufacturing Change or Addition  
8/29/1986 014Control Supplement  
7/8/1986 012Control Supplement  
3/6/1986 011Manufacturing Change or Addition  
4/22/1986 010Labeling Revision  
7/2/1985 009Labeling Revision  
7/2/1985 008Control Supplement  
4/12/1985 007Labeling Revision  
2/21/1985 006Control Supplement  
9/13/1984 005General Efficacy (MarkIV)  
12/4/1984 004Control Supplement  
3/16/1982 003Control Supplement  
11/2/1981 002Labeling Revision  
11/2/1981 001Manufacturing Change or Addition  
5/1/1981 000Approval  
 
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