DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
LOPERAMIDE HYDROCHLORIDE
FDA Application No:
(ANDA) 074091
Active Ingredient(s):
LOPERAMIDE HYDROCHLORIDE
Company:
OHM LABS
Label History
Labels are not available on this site for LOPERAMIDE HYDROCHLORIDE, (ANDA) 074091
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
10/16/2002
009
Labeling
1/17/2002
008
Facility Addition
6/21/2000
007
Control Supplement
12/28/2000
005
Labeling
5/13/1997
004
Chemistry
2/27/1998
003
Labeling
7/18/1994
002
Chemistry
6/16/1993
001
Labeling
12/10/1992
000
Approval
Therapeutic Equivalents
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