FDA's Approved Drug Products database

Drug products

  • Active Ingredient Proprietary Name Applicant NDA

Thallous Chloride Tl 201

Active Ingredient FENTANYL
Proprietary Name SUBSYS
Applicant BTCP PHARMA
Dosage Form;Route SUBLINGUAL
Strength 0.4MG
Application Type N
Product Number 3
Approval Date 2012/01/04
RX/OTC/DISCN Yes
Applicant Full Name RX
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