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) 073122
Active Ingredient(s):
LOPERAMIDE HYDROCHLORIDE
Company:
TEVA
Label History
Labels are not available on this site for LOPERAMIDE HYDROCHLORIDE, (ANDA) 073122
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
9/18/2000
018
Manufacturing Revision
8/16/1999
016
Control Supplement
12/9/1998
015
Chemistry
3/17/1998
014
Chemistry
8/28/1996
013
Chemistry
12/27/1996
012
Chemistry
12/27/1996
010
Labeling
12/27/1996
009
Chemistry
7/18/1994
008
Chemistry
3/16/1994
007
Chemistry
3/16/1994
006
Chemistry
5/27/1994
005
Chemistry
12/2/1993
003
Chemistry
8/20/1993
002
Chemistry in Effect
8/20/1993
001
Chemistry in Effect
8/30/1991
000
Approval
Therapeutic Equivalents
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