Lutathera
Active Ingredient(s): Lutetium Lu 177 DotatateFDA Approved: * January 26, 2018
Pharm Company: * ADVANCED ACCELERATOR APPLICATIONS USA INC
Category: Cancer
* This drug may consist of multiple approval dates, manufacturers, or distributors. If applicable, they would be listed below under "NDC Database Records".
Lutathera Overview
DOTA-TATE (DOTATATE,[1] DOTA-octreotate, oxodotreotide, DOTA-(Tyr3)-octreotate,[2] and DOTA-0-Tyr3-Octreotate) is an eight amino acid long peptide, with a covalently bonded DOTA bifunctional chelator. DOTA-TATE can be reacted with the radionuclides gallium-68, lutetium-177 and copper-64 to form radiopharmaceuticals for positron emission tomography (PET) imaging or radionuclide therapy. 177Lu DOTA-TATE therapy is a form of peptide receptor radionuclide therapy (...
Details May Include Instructions, Side Effects, Interactions, Etc. Drug monograph is from Wikipedia. All text is available under the terms of the GFDL (GNU Free Documentation License). Source: en.wikipedia.org/wiki/DOTA-TATE
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Lutetium Lu 177 Dotatate
- Injection: 370mbq/ml
- Solution: 10mci/ml
NDC Database Records for Lutathera: (1 result)
Sorted by National Drug Code- 69488-003 Lutathera 10 mci/Ml Intravenous Injection by Advanced Accelerator Applications USA, Inc