Visitor Monitoring Drug History: DALMANE
 
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: DALMANE
FDA Application No: (NDA) 016721
Active Ingredient(s): FLURAZEPAM HYDROCHLORIDE
Company: VALEANT PHARM INTL
 
Label History
 
Labels are not available on this site for DALMANE, (NDA) 016721
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
8/12/2002 075Manufacturing Change or Addition  
6/14/2001 074Labeling Revision Letter 
5/25/1993 072Formulation Revision  
12/31/1992 071Control Supplement  
4/25/1990 070Control Supplement  
1/16/1990 068Manufacturing Change or Addition  
11/7/1989 067Package Change  
11/9/1987 066Labeling Revision  
12/11/1984 064Package Change  
6/15/1982 063Formulation Revision  
1/28/1982 062Package Change  
12/22/1981 061Control Supplement  
12/22/1981 060Control Supplement  
11/5/1981 059Manufacturing Change or Addition  
8/4/1981 057Package Change  
7/17/1981 056Package Change  
3/26/1981 055Control Supplement  
5/6/1981 054Labeling Revision  
8/20/1980 052Control Supplement  
8/20/1980 051Control Supplement  
7/11/1980 050Package Change  
6/17/1980 049Formulation Revision  
6/17/1980 048Package Change  
2/4/1980 047Manufacturing Change or Addition  
11/9/1979 046Manufacturing Change or Addition  
9/17/1979 045Manufacturing Change or Addition  
5/1/1979 044Formulation Revision  
3/26/1979 043Formulation Revision  
7/28/1978 042Formulation Revision  
7/12/1978 041Formulation Revision  
7/20/1978 040Labeling Revision  
7/10/1978 039Labeling Revision  
5/2/1978 038Manufacturing Change or Addition  
7/12/1977 037Formulation Revision  
6/29/1977 036Control Supplement  
8/2/1977 034Distributor  
12/10/1976 032Labeling Revision  
7/10/1978 030Labeling Revision  
7/1/1975 027Control Supplement  
1/16/1975 025Control Supplement  
9/17/1974 024Control Supplement  
4/22/1974 023Final Printed Labeling (MarkIV)  
4/7/1970 000Approval Other Important Information from FDA 
 
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