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) 075560
Active Ingredient(s):
CIMETIDINE HYDROCHLORIDE
Company:
NOVEX
Label History
Labels are not available on this site for CIMETIDINE HYDROCHLORIDE, (ANDA) 075560
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
1/26/2001
003
Facility Addition
10/26/2000
002
Control Supplement
3/15/2000
000
Approval
Therapeutic Equivalents
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