DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
AMIODARONE HYDROCHLORIDE
FDA Application No:
(ANDA) 075761
Active Ingredient(s):
AMIODARONE HYDROCHLORIDE
Company:
ABRAXIS PHARM
Label History
Labels are not available on this site for AMIODARONE HYDROCHLORIDE, (ANDA) 075761
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
10/15/2002
000
Approval
Letter
Review
Other Important Information from FDA
8/23/2001
000
Tentative Approval
Letter
Review
Other Important Information from FDA
Therapeutic Equivalents
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