DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
TEGISON
FDA Application No:
(NDA) 019369
Active Ingredient(s):
ETRETINATE
Company:
ROCHE
Label History
Labels are not available on this site for TEGISON, (NDA) 019369
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
2/16/1995
011
Control Supplement
1/12/1994
010
Manufacturing Change or Addition
10/8/1991
008
Control Supplement
10/16/1990
007
Control Supplement
8/31/1988
006
Control Supplement
8/5/1988
005
Expiration Date Change
3/25/1988
004
Package Change
5/27/1988
003
Labeling Revision
4/2/1987
002
Control Supplement
4/29/1987
001
Labeling Revision
9/30/1986
000
Approval
There are no Therapeutic Equivalents
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