DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
AQUATENSEN
FDA Application No:
(NDA) 017364
Active Ingredient(s):
METHYCLOTHIAZIDE
Company:
MEDPOINTE PHARM HLC
Label History
Labels are not available on this site for AQUATENSEN, (NDA) 017364
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
6/12/1992
011
Control Supplement
3/20/1992
010
Labeling Revision
12/3/1990
009
Control Supplement
6/22/1988
008
Labeling Revision
1/24/1985
007
Control Supplement
4/28/1983
005
Formulation Revision
9/29/1987
004
Practioner Draft Labeling
10/15/1981
003
Package Change
11/26/1979
002
Manufacturing Change or Addition
1/16/1980
001
Labeling Revision
9/7/1977
000
Approval
Therapeutic Equivalents
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