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) 072335
Active Ingredient(s):
DROPERIDOL
Company:
LUITPOLD
Label History
Labels are not available on this site for DROPERIDOL, (ANDA) 072335
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
3/25/1999
009
Chemistry
10/13/1998
008
Chemistry
7/15/1998
007
Chemistry
2/17/1995
006
Labeling
2/28/1996
005
Chemistry
10/11/1994
004
Chemistry
3/8/1995
003
Chemistry
2/13/1992
001
Labeling
10/23/1988
000
Approval
Therapeutic Equivalents
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