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) 074984
Active Ingredient(s):
DILTIAZEM HYDROCHLORIDE
Company:
ACTAVIS ELIZABETH
Label History
Labels are not available on this site for DILTIAZEM HYDROCHLORIDE, (ANDA) 074984
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
11/4/2002
011
Control Supplement
7/31/2002
010
Control Supplement
2/11/2002
008
Control Supplement
11/2/2001
007
Control Supplement
10/1/2001
006
Supplier Addition
2/11/2002
005
Supplier Addition
2/15/2001
004
Control Supplement
12/14/2000
003
Control Supplement
12/14/2000
002
Facility Addition
9/18/2000
001
Control Supplement
12/20/1999
000
Approval
Letter
10/23/1998
000
Tentative Approval
Letter
Therapeutic Equivalents
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