Lutathera

Active Ingredient(s): Lutetium Lu 177 Dotatate
FDA 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 (Also known as DOTA-octreotate, oxodotreotide and DOTA-(Tyr3)-octreotate[1]/ DOTA-0-Tyr3-Octreotate) is an amino acid peptide, with a covalently bonded DOTA bifunctional chelator. DOTA-TATE can be bound with radionuclides such as gallium-68 and lutetium-177 to form radiopharmaceuticals for PET imaging or radionuclide therapy. 177Lu DOTA-TATE therapy is a form of peptide receptor radionuclide therapy (PRRT) which targets somatostatin receptors (SSR).[2][3] Contents 1 Chemistry...

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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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Possible Dosages for this and Related Drugs:

Lutetium Lu 177 Dotatate
  • Injection: 370mbq/ml
  • Solution: 10mci/ml
Note: Above list includes dosages for all drugs with the same combination of active ingredients.

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

Other drugs which contain Lutetium Lu 177 Dotatate or a similar ingredient: (1 result)





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