DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
METAHYDRIN
FDA Application No:
(NDA) 012594
Active Ingredient(s):
TRICHLORMETHIAZIDE
Company:
SANOFI AVENTIS US
Label History
Labels are not available on this site for METAHYDRIN, (NDA) 012594
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
1/28/1994
018
Labeling Revision
6/23/1989
017
Labeling Revision
6/16/1988
016
Package Change
6/16/1988
015
Manufacturing Change or Addition
6/16/1988
013
Practioner Draft Labeling
6/16/1988
008
Control Supplement
Therapeutic Equivalents
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