DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
HYDROCHLOROTHIAZIDE
FDA Application No:
(ANDA) 083972
Active Ingredient(s):
HYDROCHLOROTHIAZIDE
Company:
MUTUAL PHARM
Label History
Labels are not available on this site for HYDROCHLOROTHIAZIDE, (ANDA) 083972
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
12/1/1998
174
Chemistry
12/23/1994
173
Chemistry
10/11/1994
172
Chemistry
5/24/1994
171
Labeling
2/12/1993
170
Labeling
8/18/1992
169
Labeling
4/3/1992
168
Chemistry
4/3/1992
166
Chemistry
8/6/1990
164
Labeling
4/2/1991
163
Chemistry
4/2/1991
162
Chemistry
12/28/1989
161
Labeling
2/5/1986
153
Chemistry
2/5/1986
152
Chemistry
3/29/1985
151
Chemistry
3/29/1985
150
Chemistry
12/18/1984
149
Chemistry
12/18/1984
148
Chemistry
5/25/1982
142
Chemistry
5/25/1982
140
Chemistry
5/25/1982
109
Chemistry
10/3/1974
000
Approval
Review
Therapeutic Equivalents
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