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) 074895
Active Ingredient(s):
AMIODARONE HYDROCHLORIDE
Company:
TEVA
Label History
Labels are not available on this site for AMIODARONE HYDROCHLORIDE, (ANDA) 074895
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
7/26/2000
007
Expiration Date Change
7/26/2000
005
Labeling
7/26/2000
004
Packaging Addition
6/29/2000
003
Control Supplement
2/11/2000
002
Labeling
4/16/1999
000
Approval
Letter
Other Important Information from FDA
Therapeutic Equivalents
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