DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
DIAZEPAM
FDA Application No:
(ANDA) 070707
Active Ingredient(s):
DIAZEPAM
Company:
ACTAVIS ELIZABETH
Label History
Labels are not available on this site for DIAZEPAM, (ANDA) 070707
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
10/11/2002
015
Control Supplement
11/2/2001
014
Control Supplement
10/25/2000
013
Control Supplement
10/25/2000
012
Control Supplement
11/4/1999
011
Control Supplement
7/20/1999
010
Chemistry
1/18/1996
009
Chemistry
3/31/1993
008
Labeling in Effect
11/21/1990
007
Chemistry
3/27/1989
006
Chemistry
3/27/1989
005
Chemistry
6/7/1988
004
Labeling
1/21/1988
002
Chemistry
1/21/1988
001
Chemistry
3/19/1986
000
Approval
Therapeutic Equivalents
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