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) 074079
Active Ingredient(s):
DILTIAZEM HYDROCHLORIDE
Company:
TEVA
Label History
Labels are not available on this site for DILTIAZEM HYDROCHLORIDE, (ANDA) 074079
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
11/27/2002
008
Control Supplement
7/7/2000
007
Facility Addition
3/22/1999
006
Chemistry
6/12/1998
005
Labeling
5/12/1997
004
Labeling
1/9/1995
002
Chemistry
6/30/1994
001
Chemistry in Effect
11/30/1993
000
Approval
Therapeutic Equivalents
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