DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
PROMETHAZINE HYDROCHLORIDE
FDA Application No:
(ANDA) 084234
Active Ingredient(s):
PROMETHAZINE HYDROCHLORIDE
Company:
SANDOZ
Label History
Labels are not available on this site for PROMETHAZINE HYDROCHLORIDE, (ANDA) 084234
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
12/16/2002
054
Control Supplement
4/19/2002
053
Control Supplement
11/20/2002
052
Package Change
3/23/2001
051
Control Supplement
5/5/1999
050
Chemistry
12/15/1998
049
Chemistry
10/3/1996
048
Chemistry
12/1/1995
047
Chemistry
3/17/1995
046
Chemistry
8/28/1991
045
Labeling in Effect
11/1/1988
044
Labeling
2/11/1985
039
Chemistry
2/2/1983
035
Chemistry
3/23/1982
031
Chemistry
10/22/1982
030
Chemistry
10/22/1982
029
Chemistry
12/16/1981
028
Chemistry
10/22/1982
022
Chemistry
12/19/1975
000
Approval
Therapeutic Equivalents
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