DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
TENEX
FDA Application No:
(NDA) 019032
Active Ingredient(s):
GUANFACINE HYDROCHLORIDE
Company:
DR REDDYS LABS INC
Label History
Labels are not available on this site for TENEX, (NDA) 019032
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
3/12/2002
017
Labeling Revision
Letter
Review
3/12/2002
016
Labeling Revision
Letter
Review
1/13/1998
015
Manufacturing Change or Addition
9/17/1991
014
Control Supplement
3/1/1991
013
Manufacturing Change or Addition
11/29/1989
012
Control Supplement
2/1/1990
011
Labeling Revision
5/11/1993
010
New or Modified Indication
11/7/1988
009
Labeling Revision
6/9/1988
008
Package Change
11/7/1988
007
Control Supplement
12/28/1987
006
Package Change
11/20/1987
005
Control Supplement
4/29/1987
004
Manufacturing Change or Addition
2/17/1987
002
Package Change
2/17/1987
001
Control Supplement
10/27/1986
000
Approval
Therapeutic Equivalents
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