DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
CLONIDINE HYDROCHLORIDE
FDA Application No:
(ANDA) 070925
Active Ingredient(s):
CLONIDINE HYDROCHLORIDE
Company:
MUTUAL PHARM
Label History
Labels are not available on this site for CLONIDINE HYDROCHLORIDE, (ANDA) 070925
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
12/1/1998
015
Chemistry
6/23/1997
014
Labeling
12/23/1994
013
Chemistry
10/11/1994
012
Chemistry
4/3/1992
011
Chemistry
4/3/1992
009
Chemistry
8/3/1989
008
Labeling
4/21/1989
006
Chemistry
4/21/1989
005
Labeling
9/28/1988
004
Labeling
1/20/1988
001
Chemistry
9/4/1987
000
Approval
Therapeutic Equivalents
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