DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
CIMETIDINE HYDROCHLORIDE
FDA Application No:
(ANDA) 074428
Active Ingredient(s):
CIMETIDINE HYDROCHLORIDE
Company:
CLONMEL HLTHCARE
Label History
Labels are not available on this site for CIMETIDINE HYDROCHLORIDE, (ANDA) 074428
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
8/27/2001
002
Facility Addition
10/20/1997
001
Chemistry
4/25/1996
000
Approval
Therapeutic Equivalents
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