Visitor Monitoring Drug History: VANCERIL
 
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: VANCERIL
FDA Application No: (NDA) 017573
Active Ingredient(s): BECLOMETHASONE DIPROPIONATE
Company: SCHERING
 
Label History
 
Labels are not available on this site for VANCERIL, (NDA) 017573
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
8/30/2000 045Control Supplement  
7/26/2000 044Control Supplement  
3/11/1999 041Control Supplement  
2/8/1999 040Labeling Revision Review 
11/27/1995 039Control Supplement  
8/3/1995 038Control Supplement  
8/23/1989 036Labeling Revision  
8/2/1988 034Manufacturing Change or Addition  
9/24/1987 031Manufacturing Change or Addition  
2/1/1988 030Control Supplement  
7/8/1986 029Control Supplement  
3/6/1986 028Manufacturing Change or Addition  
2/24/1986 027Labeling Revision  
2/24/1986 026Control Supplement  
1/2/1985 024Control Supplement  
2/21/1985 023Control Supplement  
12/17/1984 021Control Supplement  
2/4/1982 019Control Supplement  
2/2/1982 018Control Supplement  
12/3/1981 017Control Supplement  
6/20/1981 016Control Supplement  
3/23/1981 015Control Supplement  
6/30/1981 014Labeling Revision  
1/13/1981 013Labeling Revision  
1/13/1981 012Manufacturing Change or Addition  
11/24/1980 011Labeling Revision  
6/23/1980 009Labeling Revision  
3/27/1979 008Distributor  
6/15/1979 007Control Supplement  
6/26/1979 006Control Supplement  
6/14/1979 005Labeling Revision  
4/6/1979 004Control Supplement  
4/13/1979 003Control Supplement  
6/14/1979 002Labeling Revision  
5/12/1976 000Approval  
 
Therapeutic Equivalents
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