FDA's Approved Drug Products database

Drug products

  • Active Ingredient Proprietary Name Applicant NDA

Thallous Chloride Tl 201

Active Ingredient NAFTIFINE HYDROCHLORIDE
Proprietary Name NAFTIN
Applicant SEBELA IRELAND LTD
Dosage Form;Route TOPICAL
Strength 0.02
Application Type N
Product Number 2
Approval Date 2012/01/13
RX/OTC/DISCN Yes
Applicant Full Name RX
TE Code AB
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