DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
DAUNORUBICIN HYDROCHLORIDE
FDA Application No:
(ANDA) 064212
Active Ingredient(s):
DAUNORUBICIN HYDROCHLORIDE
Company:
TEVA PARENTERAL
Label History
Labels are not available on this site for DAUNORUBICIN HYDROCHLORIDE, (ANDA) 064212
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
12/10/2001
005
Labeling
5/3/1999
004
Labeling
5/3/1999
003
Chemistry
5/3/1999
002
Chemistry
5/3/1999
001
Chemistry New Strength
6/23/1998
000
Approval
Letter
Therapeutic Equivalents
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