FDA's Approved Drug Products database

Drug products

  • Active Ingredient Proprietary Name Applicant NDA

Thallous Chloride Tl 201

Active Ingredient OLANZAPINE
Proprietary Name OLANZAPINE
Applicant AUROBINDO PHARMA LTD
Dosage Form;Route ORAL
Strength 10MG
Application Type A
Product Number 2
Approval Date 2014/05/15
RX/OTC/DISCN No
Applicant Full Name RX
TE Code AB
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