FDA's Approved Drug Products database

Drug products

  • Active Ingredient Proprietary Name Applicant NDA

Thallous Chloride Tl 201

Active Ingredient CARBIDOPA; LEVODOPA
Proprietary Name DUOPA
Applicant ABBVIE INC
Dosage Form;Route ENTERAL
Strength 4.63MG/ML;20MG/ML
Application Type N
Product Number 1
Approval Date 2015/01/09
RX/OTC/DISCN Yes
Applicant Full Name RX
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