FDA's Approved Drug Products database

Drug products

  • Active Ingredient Proprietary Name Applicant NDA

Thallous Chloride Tl 201

Active Ingredient LAMIVUDINE
Proprietary Name LAMIVUDINE
Applicant LANNETT CO INC
Dosage Form;Route ORAL
Strength 10MG/ML
Application Type A
Product Number 1
Approval Date 2014/10/31
RX/OTC/DISCN No
Applicant Full Name RX
TE Code AA
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