FDA's Approved Drug Products database

Drug products

  • Active Ingredient Proprietary Name Applicant NDA

Thallous Chloride Tl 201

Active Ingredient AMINOSALICYLATE SODIUM
Proprietary Name SODIUM P.A.S.
Applicant LANNETT
Dosage Form;Route ORAL
Strength 500MG
Application Type A
Product Number 2
Approval Date Approved Prior to Jan 1, 1982
RX/OTC/DISCN No
Applicant Full Name DISCN
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