Visitor Monitoring Drug History: BECLOVENT
 
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Label and Approval History

Drug Name: BECLOVENT
FDA Application No: (NDA) 018153
Active Ingredient(s): BECLOMETHASONE DIPROPIONATE
Company: GLAXOSMITHKLINE
 
Label History
 
Labels are not available on this site for BECLOVENT, (NDA) 018153
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
12/10/1997 022Labeling Revision  
7/6/1993 018Package Change  
8/10/1992 017Manufacturing Change or Addition  
11/19/1993 016Labeling Revision  
12/15/1988 015Labeling Revision  
4/27/1989 014Manufacturing Change or Addition  
3/6/1987 012Manufacturing Change or Addition  
9/10/1985 011Labeling Revision  
9/10/1985 010Package Change  
12/13/1985 009Labeling Revision  
9/15/1984 008Control Supplement  
3/1/1984 007Package Change  
3/1/1984 006Formulation Revision  
12/15/1988 005Labeling Revision  
2/16/1988 004Labeling Revision  
2/16/1988 003Control Supplement  
1/19/1982 002Labeling Revision  
1/19/1982 001Control Supplement  
6/24/1980 000Approval  
 
Therapeutic Equivalents
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