Visitor Monitoring Drug History: CORGARD
 
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: CORGARD
FDA Application No: (NDA) 018063
Active Ingredient(s): NADOLOL
Company: KING PHARMS
 
Label History
 
Labels are not available on this site for CORGARD, (NDA) 018063
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
9/19/2001 058Manufacturing Change or Addition  
3/18/1996 057Control Supplement  
8/16/1995 056Manufacturing Change or Addition  
4/5/1994 055Control Supplement  
5/1/1992 054Formulation Revision  
5/20/1992 053Manufacturing Change or Addition  
11/8/1991 052Manufacturing Change or Addition  
5/3/1991 051Control Supplement  
3/29/1991 050Manufacturing Change or Addition  
11/7/1990 049Labeling Revision  
9/3/1987 048Package Change  
8/21/1990 047Control Supplement  
1/6/1987 046Package Change  
3/11/1987 045Expiration Date Change  
8/19/1986 043Control Supplement  
10/7/1986 042Control Supplement  
5/15/1985 040Labeling Revision  
10/24/1984 039Package Change  
8/6/1984 038Control Supplement  
5/16/1984 037Control Supplement  
5/15/1984 036Control Supplement  
10/28/1986 035New Dosage Regimen  
5/16/1984 034Expiration Date Change  
3/6/1984 033Package Change  
2/8/1984 032Package Change  
1/17/1984 031Control Supplement  
11/16/1984 030General Efficacy (MarkIV)  
11/1/1983 029Expiration Date Change  
10/14/1983 028Control Supplement  
7/21/1983 027Control Supplement  
3/29/1983 026Control Supplement  
3/29/1983 024Manufacturing Change or Addition  
11/18/1982 023Package Change  
9/22/1982 022Manufacturing Change or Addition  
10/1/1982 021Control Supplement  
6/2/1982 019Control Supplement  
4/1/1982 018Control Supplement  
3/2/1982 017Control Supplement  
10/15/1981 016Expiration Date Change  
8/28/1981 015Control Supplement  
7/24/1981 014Formulation Revision  
7/9/1981 013Formulation Revision  
4/2/1981 012Control Supplement  
8/28/1981 011Package Change  
1/27/1981 010Package Change  
3/17/1981 009Control Supplement  
12/30/1980 008Labeling Revision  
10/22/1980 005Control Supplement  
1/27/1981 004Formulation Revision  
8/14/1980 003Manufacturing Change or Addition  
2/11/1980 002Labeling Revision  
2/11/1980 001Labeling Revision  
12/10/1979 000Approval  
 
Therapeutic Equivalents
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