FDA's Approved Drug Products database

Drug products

  • Active Ingredient Proprietary Name Applicant NDA

Thallous Chloride Tl 201

Active Ingredient TADALAFIL
Proprietary Name CIALIS
Applicant LILLY
Dosage Form;Route ORAL
Strength 20MG
Application Type N
Product Number 3
Approval Date 2003/11/21
RX/OTC/DISCN Yes
Applicant Full Name RX
TE Code AB1
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