FDA's Approved Drug Products database

Drug products

  • Active Ingredient Proprietary Name Applicant NDA

Thallous Chloride Tl 201

Active Ingredient MESORIDAZINE BESYLATE
Proprietary Name SERENTIL
Applicant NOVARTIS
Dosage Form;Route ORAL
Strength EQ 100MG BASE **Federal Register determination that product was not discontinued or withdrawn for sa
Application Type N
Product Number 4
Approval Date Approved Prior to Jan 1, 1982
RX/OTC/DISCN No
Applicant Full Name DISCN
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