FDA's Approved Drug Products database

Drug products

  • Active Ingredient Proprietary Name Applicant NDA

Thallous Chloride Tl 201

Active Ingredient SODIUM NITRITE
Proprietary Name SODIUM NITRITE
Applicant HOPE PHARMS
Dosage Form;Route INTRAVENOUS
Strength 300MG/10ML (30MG/ML)
Application Type N
Product Number 1
Approval Date 2012/02/14
RX/OTC/DISCN Yes
Applicant Full Name RX
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