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) 018062
Active Ingredient(s): ALBUTEROL SULFATE
Company: SCHERING
 
Label History
 
Labels are not available on this site for PROVENTIL, (NDA) 018062
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
8/12/1999 019Control Supplement  
8/18/1998 018Control Supplement  
11/6/1998 016Labeling Revision  
9/9/1996 015Manufacturing Change or Addition  
5/27/1993 011Control Supplement  
1/24/1989 009Manufacturing Change or Addition  
11/19/1986 007Package Change  
7/8/1986 006Control Supplement  
12/4/1984 005Control Supplement  
4/12/1985 004General Efficacy (MarkIV)  
5/16/1985 002Labeling Revision  
5/16/1985 001Control Supplement  
1/19/1983 000Approval  
 
Therapeutic Equivalents
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