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 SUN PHARM INDUSTRIES
Dosage Form;Route ORAL
Strength 80MG
Application Type A
Product Number 1
Approval Date 2001/10/15
RX/OTC/DISCN No
Applicant Full Name DISCN
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