DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
CLORAZEPATE DIPOTASSIUM
FDA Application No:
(ANDA) 071742
Active Ingredient(s):
CLORAZEPATE DIPOTASSIUM
Company:
CLONMEL HLTHCARE
Label History
Labels are not available on this site for CLORAZEPATE DIPOTASSIUM, (ANDA) 071742
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
7/2/1993
002
Labeling
8/23/1989
001
Labeling
12/14/1987
000
Approval
Therapeutic Equivalents
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