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) 017853
Active Ingredient(s): ALBUTEROL SULFATE
Company: SCHERING
 
Label History
 
Labels are not available on this site for PROVENTIL, (NDA) 017853
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
8/12/1999 020Control Supplement  
8/10/1998 018Control Supplement  
11/6/1998 016Labeling Revision Review 
9/9/1996 015Manufacturing Change or Addition  
12/15/1992 012Manufacturing Change or Addition  
1/24/1989 010Manufacturing Change or Addition  
7/8/1986 008Control Supplement  
12/24/1985 007Labeling Revision  
12/24/1985 006Labeling Revision  
12/4/1984 005Control Supplement  
3/16/1986 003Formulation Revision  
5/24/1985 001Labeling Revision  
5/7/1982 000Approval  
 
Therapeutic Equivalents
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