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) 071620
Active Ingredient(s):
TEMAZEPAM
Company:
ACTAVIS ELIZABETH
Label History
Labels are not available on this site for TEMAZEPAM, (ANDA) 071620
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
12/12/2002
015
Control Supplement
11/2/2001
014
Control Supplement
2/1/2001
013
Labeling
1/18/1996
012
Chemistry
7/9/1993
011
Labeling
12/28/1992
010
Labeling
10/21/1992
009
Chemistry
3/21/1990
008
SBA
8/8/1989
006
SBA
9/25/1991
006
Chemistry
9/25/1991
005
Chemistry
6/7/1989
003
Chemistry
12/20/1988
002
Labeling
10/5/1987
001
Chemistry
8/7/1987
000
Approval
Therapeutic Equivalents
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