DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
PROMETHAZINE PLAIN
FDA Application No:
(ANDA) 087953
Active Ingredient(s):
PROMETHAZINE HYDROCHLORIDE
Company:
MORTON GROVE
Label History
Labels are not available on this site for PROMETHAZINE PLAIN, (ANDA) 087953
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
2/17/2000
032
Package Change
2/17/2000
031
Control Supplement
2/17/2000
030
Expiration Date Change
2/17/2000
029
Labeling
2/17/2000
028
Chemistry
6/5/1995
022
Labeling
8/10/1994
021
Labeling
2/11/1992
020
Labeling in Effect
1/18/1991
019
Labeling
1/19/1990
018
Labeling
3/15/1989
017
Chemistry
3/16/1987
011
Chemistry
2/20/1985
007
Chemistry
2/20/1985
006
Chemistry
2/20/1985
005
Chemistry
2/20/1985
004
Chemistry
2/20/1985
003
Chemistry
2/20/1985
002
Chemistry
1/16/1985
001
Chemistry
11/15/1982
000
Approval
Therapeutic Equivalents
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