Visitor Monitoring Drug History: VALIUM
 
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: VALIUM
FDA Application No: (NDA) 013263
Active Ingredient(s): DIAZEPAM
Company: ROCHE
 
Label History
 
Labels are not available on this site for VALIUM, (NDA) 013263
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
2/12/2002 086Control Supplement Letter
Review 
11/8/2001 085Package Change  
10/25/2001 084Manufacturing Change or Addition  
5/9/2001 082Manufacturing Change or Addition Letter
Review 
8/30/2000 081Manufacturing Change or Addition Review 
9/4/1998 079Control Supplement  
9/19/1997 078Package Change  
11/5/1997 077Manufacturing Change or Addition  
9/5/1997 076Control Supplement  
2/7/2002 075Labeling Revision Letter
Review 
10/26/1989 074Manufacturing Change or Addition  
11/8/1988 073Manufacturing Change or Addition  
2/7/2002 072Labeling Revision Letter
Review 
1/20/1988 071Control Supplement  
8/27/1986 070Expiration Date Change  
4/16/1985 069Manufacturing Change or Addition  
1/13/1984 068Control Supplement  
1/13/1984 067Labeling Revision  
1/20/1983 066Control Supplement  
1/20/1983 065Control Supplement  
12/10/1982 064Package Change  
11/30/1982 063Package Change  
10/18/1982 062Labeling Revision  
10/18/1982 061Package Change  
10/18/1982 060Package Change  
10/18/1982 059Package Change  
8/11/1982 057Control Supplement  
5/11/1982 056Control Supplement  
3/4/1983 055Expiration Date Change  
3/26/1981 054Labeling Revision  
7/17/1981 053Manufacturing Change or Addition  
10/14/1980 051Control Supplement  
6/17/1980 050Package Change  
5/19/1980 049Labeling Revision  
1/9/1981 048Formulation Revision  
9/20/1979 047Formulation Revision  
11/2/1979 046Labeling Revision  
4/4/1979 045Package Change  
2/26/1980 044Control Supplement  
3/30/1978 043Labeling Revision  
9/21/1977 042Labeling Revision  
12/14/1976 041Labeling Revision  
10/27/1976 040Labeling Revision  
8/27/1976 039Labeling Revision  
8/25/1975 038Control Supplement  
6/18/1975 037Control Supplement  
1/24/1975 036Control Supplement  
12/13/1974 034Control Supplement  
11/15/1963 000Approval  
 
Therapeutic Equivalents
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