DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
DILTIAZEM HYDROCHLORIDE
FDA Application No:
(ANDA) 072838
Active Ingredient(s):
DILTIAZEM HYDROCHLORIDE
Company:
MYLAN
Label History
Labels are not available on this site for DILTIAZEM HYDROCHLORIDE, (ANDA) 072838
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
4/12/2007
011
Control Supplement
7/12/1999
007
Chemistry
12/12/1996
006
Labeling
7/13/1995
005
Labeling
8/29/1995
004
Labeling
8/29/1995
003
Chemistry
12/13/1993
002
Labeling
11/5/1992
000
Approval
3/16/1992
000
Tentative Approval
Therapeutic Equivalents
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