DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
DEMULEN 1/35-28
FDA Application No:
(NDA) 018160
Active Ingredient(s):
ETHINYL ESTRADIOL; ETHYNODIOL DIACETATE
Company:
GD SEARLE LLC
Label History
Labels are not available on this site for DEMULEN 13528, (NDA) 018160
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
12/27/1996
031
Formulation Revision
9/2/1999
030
Labeling Revision
4/20/1994
029
Labeling Revision
4/28/1993
028
Labeling Revision
12/16/1991
027
Control Supplement
8/7/1991
026
Package Change
10/28/1988
022
Control Supplement
11/14/1991
019
Labeling Revision
10/23/1986
017
Labeling Revision
6/10/1986
016
Labeling Revision
3/13/1986
015
Labeling Revision
6/3/1985
014
Labeling Revision
9/18/1985
013
Expiration Date Change
4/5/1985
012
Labeling Revision
2/12/1985
011
Labeling Revision
9/18/1984
010
Labeling Revision
3/6/1984
008
Labeling Revision
6/3/1983
005
Control Supplement
6/9/1983
004
Control Supplement
11/22/1982
002
Control Supplement
12/30/1981
000
Approval
There are no Therapeutic Equivalents
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