DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
AMIODARONE HYDROCHLORIDE
FDA Application No:
(ANDA) 076299
Active Ingredient(s):
AMIODARONE HYDROCHLORIDE
Company:
BEDFORD LABS
Original Approval or Tentative Approval Date:
October 24, 2002
Therapeutic Equivalents
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Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
AMIODARONE HYDROCHLORIDE
AMIODARONE HYDROCHLORIDE
50MG/ML
INJECTABLE; INJECTION
Prescription
Yes
AP
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