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) 071785
Active Ingredient(s):
CLONIDINE HYDROCHLORIDE
Company:
CLONMEL HLTHCARE
Label History
Labels are not available on this site for CLONIDINE HYDROCHLORIDE, (ANDA) 071785
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
9/18/2000
011
Manufacturing Revision
5/18/1998
010
Chemistry
2/18/1997
009
Labeling
11/13/1996
008
Chemistry
7/26/1994
007
Chemistry
1/3/1990
006
Labeling
10/18/1989
005
Labeling
5/12/1988
002
Labeling
5/12/1988
001
Chemistry
4/5/1988
000
Approval
Therapeutic Equivalents
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