DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
RESERPINE, HYDRALAZINE HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE
FDA Application No:
(ANDA) 085549
Active Ingredient(s):
HYDRALAZINE HYDROCHLORIDE; HYDROCHLOROTHIAZIDE; RESERPINE
Company:
WATSON LABS
Label History
Labels are not available on this site for RESERPINE, HYDRALAZINE HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE, (ANDA) 085549
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
8/11/1993
046
Labeling
4/14/1992
045
Labeling
11/1/1991
044
Labeling
11/19/1990
043
Chemistry
7/3/1991
042
Chemistry
6/29/1990
041
Chemistry
4/25/1989
040
Labeling
1/23/1989
039
Labeling
8/5/1988
038
Chemistry
8/5/1988
037
Chemistry
8/5/1988
036
Chemistry
11/30/1984
033
Chemistry
8/10/1984
031
Chemistry
4/22/1983
029
Chemistry
8/19/1982
024
Chemistry
9/29/1977
000
Approval
There are no Therapeutic Equivalents
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