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) 074991
Active Ingredient(s):
LOPERAMIDE HYDROCHLORIDE
Company:
DURAMED PHARMS BARR
Label History
Labels are not available on this site for LOPERAMIDE HYDROCHLORIDE, (ANDA) 074991
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
12/29/1997
000
Approval
Therapeutic Equivalents
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