Visitor Monitoring Drug History: NOR-QD
 
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: NOR-QD
FDA Application No: (NDA) 017060
Active Ingredient(s): NORETHINDRONE
Company: WATSON LABS (UTAH)
 
Label History
 
Labels are not available on this site for NORQD, (NDA) 017060
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
10/20/2005 067Labeling Revision Letter 
9/30/1999 066Manufacturing Change or Addition  
2/24/1999 065Manufacturing Change or Addition  
11/30/1999 064Labeling Revision  
12/11/1996 063Labeling Revision  
5/23/1995 062Labeling Revision  
5/26/1995 061Labeling Revision  
9/19/1990 059Package Change  
11/2/1990 058Labeling Revision  
10/22/1986 056Final Printed Labeling - MarkIV  
10/25/1985 055Labeling Revision  
6/19/1985 054Labeling Revision  
11/13/1984 052Manufacturing Change or Addition  
6/12/1984 051Labeling Revision  
9/27/1984 050Control Supplement  
7/26/1983 049Control Supplement  
7/19/1983 048Control Supplement  
7/19/1983 047Control Supplement  
4/28/1984 046Labeling Revision  
7/26/1983 045Control Supplement  
6/13/1983 044Control Supplement  
7/29/1982 041Control Supplement  
5/20/1980 037Control Supplement  
7/18/1979 036Manufacturing Change or Addition  
7/18/1979 033Control Supplement  
11/6/1978 029Control Supplement  
11/6/1978 028Control Supplement  
5/26/1978 027Control Supplement  
7/1/1977 018Distributor  
7/1/1977 017Distributor  
1/2/1981 016Labeling Revision  
6/25/1976 013Control Supplement  
5/16/1975 010Labeling Revision  
5/16/1975 008Control Supplement  
5/16/1975 006Control Supplement  
1/2/1973 000Approval  
 
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