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) 071135
Active Ingredient(s):
DIAZEPAM
Company:
WATSON LABS
Label History
Labels are not available on this site for DIAZEPAM, (ANDA) 071135
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
4/25/2001
014
Control Supplement
6/21/2001
013
Control Supplement
10/17/1997
011
Chemistry
1/28/1991
010
Chemistry
7/2/1993
010
Labeling in Effect
5/31/1991
009
Chemistry
6/29/1990
008
Chemistry
1/25/1989
007
SBA
7/10/1990
007
Chemistry
7/10/1990
006
Chemistry
5/4/1988
004
Labeling
8/11/1988
002
Chemistry
2/3/1987
000
Approval
Therapeutic Equivalents
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