DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
PROMETHEGAN
FDA Application No:
(ANDA) 087165
Active Ingredient(s):
PROMETHAZINE HYDROCHLORIDE
Company:
G AND W LABS
Label History
Labels are not available on this site for PROMETHEGAN, (ANDA) 087165
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
11/4/2002
011
Control Supplement
3/4/1999
007
Chemistry
12/1/1993
004
Chemistry
11/8/1991
003
Labeling
5/15/1991
002
Labeling
7/23/1991
001
Labeling
8/14/1987
000
Approval
Therapeutic Equivalents
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