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) 075116
Active Ingredient(s):
DILTIAZEM HYDROCHLORIDE
Company:
BIOVAIL
Label History
Labels are not available on this site for DILTIAZEM HYDROCHLORIDE, (ANDA) 075116
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
10/3/2002
006
Facility Addition
5/20/2002
004
Control Supplement
4/20/2001
003
Facility Addition
10/5/2000
002
Control Supplement
12/23/1999
000
Approval
Letter
10/22/1999
000
Tentative Approval
Letter
Therapeutic Equivalents
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