DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
CIMETIDINE
FDA Application No:
(ANDA) 074339
Active Ingredient(s):
CIMETIDINE
Company:
CLONMEL HLTHCARE
Label History
Labels are not available on this site for CIMETIDINE, (ANDA) 074339
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
7/18/2002
005
Packager Addition
8/27/2001
004
Facility Addition
5/14/1996
001
Chemistry
6/23/1995
000
Approval
Therapeutic Equivalents
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