DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
DOPAMINE HYDROCHLORIDE
FDA Application No:
(ANDA) 070799
Active Ingredient(s):
DOPAMINE HYDROCHLORIDE
Company:
LUITPOLD
Label History
Labels are not available on this site for DOPAMINE HYDROCHLORIDE, (ANDA) 070799
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
10/30/2001
011
Labeling
11/7/1997
010
Labeling
1/9/1998
009
Chemistry
9/24/1996
008
Labeling
2/28/1996
007
Chemistry
6/30/1993
006
Chemistry in Effect
10/27/1992
005
Labeling in Effect
8/26/1992
004
Labeling
6/30/1989
003
Chemistry
2/5/1992
002
Chemistry
6/30/1989
001
Chemistry
2/11/1987
000
Approval
Therapeutic Equivalents
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