Visitor Monitoring Drug History: PARLODEL
 
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: PARLODEL
FDA Application No: (NDA) 017962
Active Ingredient(s): BROMOCRIPTINE MESYLATE
Company: NOVARTIS
 
Label History
 
View the label approved on November 17, 2005 for PARLODEL, (NDA) 017962


To see older, previously-approved labels, go to the "Approval History" section of this page. Older labels are for historical information only and should not be used for clinical purposes.
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
11/9/2005 064Labeling Revision Letter
Label
Review 
11/9/2005 063Labeling Revision Letter
Label
Review 
2/21/2002 062Manufacturing Change or Addition  
11/20/2001 061Manufacturing Change or Addition  
5/22/2001 060Control Supplement  
5/1/2000 059Manufacturing Change or Addition  
10/1/1999 058Manufacturing Change or Addition  
9/10/1999 057Manufacturing Change or Addition  
4/22/1999 056Package Change  
9/3/1998 055Manufacturing Change or Addition  
8/13/1998 054Manufacturing Change or Addition  
11/9/1999 053Labeling Revision  
4/2/1998 052Labeling Revision  
7/3/1996 051Labeling Revision  
11/28/1995 050Manufacturing Change or Addition  
10/10/1995 049Control Supplement  
3/24/1995 048Labeling Revision  
2/8/1995 047Labeling Revision  
6/9/1995 046Control Supplement  
7/29/1994 045Package Change  
3/13/1995 044Control Supplement  
5/25/1994 042Labeling Revision  
4/1/1993 040Manufacturing Change or Addition  
4/1/1993 039Package Change  
5/29/1992 038Labeling Revision  
12/11/1991 037Labeling Revision  
5/29/1992 036Labeling Revision  
6/9/1992 035Control Supplement  
10/22/1990 034Control Supplement  
10/22/1990 033Control Supplement  
10/22/1990 032Control Supplement  
3/2/1989 030Control Supplement  
12/19/1989 029Package Change  
6/4/1990 028Package Change  
12/31/1991 027Labeling Revision  
7/1/1987 025Labeling Revision  
1/28/1987 022Labeling Revision  
1/21/1987 021Control Supplement  
9/17/1985 020Control Supplement  
12/14/1984 019Labeling Revision  
6/28/1985 018General Efficacy (MarkIV)  
11/30/1983 017Control Supplement  
7/29/1982 016Control Supplement  
7/29/1982 015Control Supplement  
8/26/1982 014Control Supplement  
2/16/1984 013Control Supplement  
6/11/1981 012Manufacturing Change or Addition  
3/1/1982 011Control Supplement  
12/14/1984 010Labeling Revision  
2/6/1981 009Package Change  
2/4/1981 008Package Change  
7/29/1982 007Control Supplement  
9/23/1981 006Other Amendment  
5/17/1979 004Package Change  
2/27/1979 003Manufacturing Change or Addition  
2/16/1979 002Control Supplement  
2/7/1980 001Manufacturing Change or Addition  
6/28/1978 000Approval  
 
Therapeutic Equivalents
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