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) 072999
Active Ingredient(s):
DOPAMINE HYDROCHLORIDE
Company:
TEVA PARENTERAL
Label History
Labels are not available on this site for DOPAMINE HYDROCHLORIDE, (ANDA) 072999
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
6/21/2001
003
Labeling
4/23/1998
002
Labeling
9/9/1997
001
Labeling
10/23/1991
000
Approval
Therapeutic Equivalents
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