DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
DROPERIDOL
FDA Application No:
(ANDA) 072123
Active Ingredient(s):
DROPERIDOL
Company:
LUITPOLD
Label History
Labels are not available on this site for DROPERIDOL, (ANDA) 072123
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
1/10/2002
012
Labeling
3/25/1999
008
Chemistry
7/2/1998
007
Chemistry
2/17/1995
005
Labeling
2/28/1996
004
Chemistry
10/11/1994
003
Chemistry
5/26/1995
002
Chemistry
10/24/1988
000
Approval
Therapeutic Equivalents
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