FDA's Approved Drug Products database

Drug products

  • Active Ingredient Proprietary Name Applicant NDA

Thallous Chloride Tl 201

Active Ingredient ESZOPICLONE
Proprietary Name LUNESTA
Applicant SUNOVION PHARMS INC
Dosage Form;Route ORAL
Strength 1MG
Application Type N
Product Number 1
Approval Date 2004/12/15
RX/OTC/DISCN No
Applicant Full Name RX
TE Code AB
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