FDA's Approved Drug Products database

Drug products

  • Active Ingredient Proprietary Name Applicant NDA

Thallous Chloride Tl 201

Active Ingredient SOTALOL HYDROCHLORIDE
Proprietary Name SOTALOL HYDROCHLORIDE
Applicant OXFORD PHARMS
Dosage Form;Route ORAL
Strength 160MG
Application Type A
Product Number 3
Approval Date 2003/11/07
RX/OTC/DISCN No
Applicant Full Name RX
TE Code AB
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