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) 074852
Active Ingredient(s):
DILTIAZEM HYDROCHLORIDE
Company:
ANDRX
Label History
Labels are not available on this site for DILTIAZEM HYDROCHLORIDE, (ANDA) 074852
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
12/24/2002
007
Packager Addition
10/11/2002
006
Packager Addition
2/15/2001
005
Control Supplement
8/16/2000
004
Control Supplement
5/16/2000
003
Control Supplement
4/7/1999
002
Chemistry
4/7/1999
001
Chemistry
10/10/1997
000
Approval
Therapeutic Equivalents
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