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) 074176
Active Ingredient(s):
CIMETIDINE HYDROCHLORIDE
Company:
ACTAVIS MID ATLANTIC
Label History
Labels are not available on this site for CIMETIDINE HYDROCHLORIDE, (ANDA) 074176
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
8/9/2000
007
Package Change
5/26/2000
006
Expiration Date Change
2/10/1997
004
Chemistry
4/24/1996
003
Labeling
2/23/1995
002
Chemistry
11/3/1994
001
Labeling
6/1/1994
000
Approval
Therapeutic Equivalents
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