FDA's Approved Drug Products database

Drug products

  • Active Ingredient Proprietary Name Applicant NDA

Thallous Chloride Tl 201

Active Ingredient DRONEDARONE HYDROCHLORIDE
Proprietary Name MULTAQ
Applicant SANOFI AVENTIS US
Dosage Form;Route ORAL
Strength EQ 400MG BASE
Application Type N
Product Number 1
Approval Date 2009/07/01
RX/OTC/DISCN Yes
Applicant Full Name RX
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