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) 085252
Active Ingredient(s):
MECLIZINE HYDROCHLORIDE
Company:
ABC HOLDING
Label History
Labels are not available on this site for MECLIZINE HYDROCHLORIDE, (ANDA) 085252
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
11/30/1990
041
Labeling
6/27/1988
040
Chemistry
4/9/1984
038
Chemistry
6/29/1983
037
Chemistry
2/15/1977
000
Approval
Therapeutic Equivalents
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