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) 074617
Active Ingredient(s):
DILTIAZEM HYDROCHLORIDE
Company:
BEDFORD
Label History
Labels are not available on this site for DILTIAZEM HYDROCHLORIDE, (ANDA) 074617
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
4/3/2001
010
Microbiology
4/12/2000
009
Labeling
6/28/2000
008
Control Supplement
3/30/2000
007
Chemistry
3/30/2000
006
Chemistry
3/30/2000
005
Chemistry
3/30/2000
004
Labeling
3/30/2000
003
Chemistry New Strength
4/29/1997
002
Chemistry
9/27/1996
001
Labeling
2/28/1996
000
Approval
Therapeutic Equivalents
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