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) 089674
Active Ingredient(s):
MECLIZINE HYDROCHLORIDE
Company:
PAR PHARM
Label History
Labels are not available on this site for MECLIZINE HYDROCHLORIDE, (ANDA) 089674
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
10/5/1998
005
Labeling
11/26/1997
004
Chemistry
11/26/1997
003
Chemistry
7/25/1995
002
Chemistry
7/13/1988
001
Labeling
3/31/1988
000
Approval
Therapeutic Equivalents
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