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) 074093
Active Ingredient(s):
DILTIAZEM HYDROCHLORIDE
Company:
CLONMEL HLTHCARE
Label History
Labels are not available on this site for DILTIAZEM HYDROCHLORIDE, (ANDA) 074093
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
10/4/1999
014
Chemistry
1/29/1998
013
Chemistry
1/28/1997
012
Labeling
1/16/1997
011
Labeling
12/11/1996
010
Chemistry
4/29/1996
009
Chemistry
11/15/1995
008
Labeling
11/7/1995
007
Chemistry
11/7/1995
006
Chemistry
2/8/1995
005
Chemistry
11/23/1994
004
Chemistry
11/23/1994
003
Chemistry
4/28/1994
002
Chemistry
5/10/1994
001
Labeling
11/5/1992
000
Approval
8/25/1992
000
Tentative Approval
Therapeutic Equivalents
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