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) 085253
Active Ingredient(s):
MECLIZINE HYDROCHLORIDE
Company:
ABC HOLDING
Label History
Labels are not available on this site for MECLIZINE HYDROCHLORIDE, (ANDA) 085253
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
11/16/1990
040
Labeling
6/27/1988
039
Chemistry
4/6/1984
036
Chemistry
6/29/1983
035
Chemistry
3/8/1983
034
Chemistry
2/7/1977
000
Approval
Therapeutic Equivalents
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