DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
TEMAZEPAM
FDA Application No:
(ANDA) 071638
Active Ingredient(s):
TEMAZEPAM
Company:
ACTAVIS ELIZABETH
Label History
Labels are not available on this site for TEMAZEPAM, (ANDA) 071638
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
12/12/2002
014
Control Supplement
11/2/2001
013
Control Supplement
2/1/2001
012
Labeling
1/18/1996
011
Chemistry
7/9/1993
010
Labeling
12/28/1992
009
Labeling
3/21/1990
008
SBA
6/26/1989
007
SBA
9/25/1991
006
Chemistry
6/6/1989
004
Chemistry
12/20/1988
003
Labeling
10/5/1987
001
Chemistry
8/7/1987
000
Approval
Therapeutic Equivalents
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