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) 074352
Active Ingredient(s):
LOPERAMIDE HYDROCHLORIDE
Company:
HI TECH PHARMA
Label History
Labels are not available on this site for LOPERAMIDE HYDROCHLORIDE, (ANDA) 074352
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
3/19/2001
002
Labeling
3/19/2001
001
Formulation Revision
11/17/1995
000
Approval
Therapeutic Equivalents
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