DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
TERAZOSIN HYDROCHLORIDE
FDA Application No:
(ANDA) 074823
Active Ingredient(s):
TERAZOSIN HYDROCHLORIDE
Company:
SANDOZ
Label History
Labels are not available on this site for TERAZOSIN HYDROCHLORIDE, (ANDA) 074823
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
10/1/2002
011
Labeling
3/5/2002
009
Control Supplement
4/19/2002
008
Control Supplement
11/6/2001
007
Control Supplement
6/7/2001
006
Control Supplement
6/28/2000
005
Control Supplement
6/18/1999
004
Chemistry
9/7/1999
003
Labeling
9/7/1999
002
Package Change
6/18/1999
001
Chemistry
3/30/1998
000
Approval
Review
Therapeutic Equivalents
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