FDA's Approved Drug Products database

Drug products

  • Active Ingredient Proprietary Name Applicant NDA

Thallous Chloride Tl 201

Active Ingredient NATEGLINIDE
Proprietary Name STARLIX
Applicant NOVARTIS
Dosage Form;Route ORAL
Strength 120MG **Federal Register determination that product was not discontinued or withdrawn for safety or
Application Type N
Product Number 2
Approval Date 2000/12/22
RX/OTC/DISCN No
Applicant Full Name DISCN
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