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) 074067
Active Ingredient(s):
DILTIAZEM HYDROCHLORIDE
Company:
TEVA PHARMS
Label History
Labels are not available on this site for DILTIAZEM HYDROCHLORIDE, (ANDA) 074067
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
3/23/1999
013
Chemistry
6/11/1998
012
Chemistry
11/25/1996
011
Labeling
7/2/1996
010
Labeling
5/31/1996
009
Chemistry
12/13/1995
008
Labeling
4/25/1995
007
Labeling
11/12/1993
006
Labeling
9/1/1993
005
Chemistry
8/8/1994
004
Chemistry
9/1/1993
003
Chemistry
9/1/1993
002
Labeling
9/1/1993
001
Chemistry
11/5/1992
000
Approval
6/30/1992
000
Tentative Approval
Therapeutic Equivalents
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