FDA's Approved Drug Products database

Drug products

  • Active Ingredient Proprietary Name Applicant NDA

Thallous Chloride Tl 201

Active Ingredient ELTROMBOPAG OLAMINE
Proprietary Name PROMACTA
Applicant NOVARTIS
Dosage Form;Route ORAL
Strength EQ 50MG ACID
Application Type N
Product Number 2
Approval Date 2008/11/20
RX/OTC/DISCN No
Applicant Full Name RX
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