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) 074345
Active Ingredient(s):
CIMETIDINE HYDROCHLORIDE
Company:
HOSPIRA
Label History
Labels are not available on this site for CIMETIDINE HYDROCHLORIDE, (ANDA) 074345
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
10/25/2002
007
Microbiology
5/5/1998
006
Microbiology
7/26/1996
005
Labeling
10/3/1996
004
Microbiology
12/22/1995
002
Labeling
1/31/1995
000
Approval
Therapeutic Equivalents
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