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) 083177
Active Ingredient(s):
HYDROCHLOROTHIAZIDE
Company:
IVAX PHARMS
Label History
Labels are not available on this site for HYDROCHLOROTHIAZIDE, (ANDA) 083177
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
7/29/2002
197
Facility Addition
11/15/2002
196
Package Change
9/12/2001
195
Packager Addition
8/22/2002
193
Control Supplement
2/3/2000
192
Labeling
1/28/2000
191
Facility Addition
2/3/2000
190
Package Change
4/30/1999
188
Chemistry
4/30/1999
187
Chemistry
4/30/1999
186
Chemistry
12/9/1998
185
Chemistry
5/13/1998
184
Chemistry
1/13/1998
183
Chemistry
5/30/1997
182
Chemistry
4/24/1996
181
Chemistry
8/17/1995
180
Labeling
6/3/1993
179
Labeling
3/12/1993
178
Labeling
10/6/1995
177
Chemistry in Effect
9/9/1992
176
Chemistry in Effect
9/9/1992
175
Chemistry in Effect
11/10/1988
174
SBA
3/31/1988
170
Chemistry
3/31/1988
169
Chemistry
6/29/1987
168
Chemistry
1/14/1987
166
Chemistry
1/14/1987
165
Chemistry
2/20/1987
164
Chemistry
3/30/1982
158
Chemistry
3/30/1982
157
Chemistry
3/30/1982
156
Chemistry
1/12/1973
000
Approval
Therapeutic Equivalents
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