DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
MECLIZINE HYDROCHLORIDE
FDA Application No:
(ANDA) 085740
Active Ingredient(s):
MECLIZINE HYDROCHLORIDE
Company:
WATSON LABS
Label History
Labels are not available on this site for MECLIZINE HYDROCHLORIDE, (ANDA) 085740
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
4/13/1999
029
Chemistry
4/13/1999
028
Chemistry
3/25/1998
027
Chemistry
3/25/1998
026
Chemistry
5/23/1997
025
Chemistry
3/28/1989
023
SBA
4/18/1989
021
Chemistry
4/18/1989
020
Chemistry
4/18/1989
019
Chemistry
5/9/1988
018
Labeling
6/24/1987
015
Chemistry
6/24/1987
014
Chemistry
5/10/1982
010
Chemistry
5/10/1982
009
Chemistry
5/10/1982
008
Chemistry
5/10/1982
004
Chemistry
7/6/1977
000
Approval
Therapeutic Equivalents
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