DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
BUPROPION HYDROCHLORIDE
FDA Application No:
(ANDA) 075491
Active Ingredient(s):
BUPROPION HYDROCHLORIDE
Company:
MYLAN
Label History
Labels are not available on this site for BUPROPION HYDROCHLORIDE, (ANDA) 075491
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
8/26/2002
002
Labeling
4/17/2000
000
Approval
Letter
Review
Other Important Information from FDA
Therapeutic Equivalents
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