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) 071136
Active Ingredient(s):
DIAZEPAM
Company:
WATSON LABS
Label History
Labels are not available on this site for DIAZEPAM, (ANDA) 071136
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
4/25/2001
015
Control Supplement
6/21/2001
014
Control Supplement
10/17/1997
012
Chemistry
7/2/1993
011
Labeling in Effect
1/28/1991
010
Chemistry
5/31/1991
009
Chemistry
6/29/1990
008
Chemistry
7/18/1988
007
Chemistry
7/18/1988
006
Chemistry
7/18/1988
005
Chemistry
5/4/1988
004
Labeling
8/11/1988
002
Chemistry
2/3/1987
000
Approval
Therapeutic Equivalents
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