Turalio

Active Ingredient(s): Pexidartinib Hydrochloride
FDA Approved: * August 2, 2019
Pharm Company: * DAIICHI SANKYO INC

* This drug may consist of multiple approval dates, manufacturers, or distributors. If applicable, they would be listed below under "NDC Database Records".



Turalio Overview

Pexidartinib (trade name Turalio; development code name PLX-3397) is a CSF1R antagonist drug created by Plexxikon[1][2] On 2 August 2019 it was approved by U.S. FDA for treatment of Giant-cell tumor of the tendon sheath (GC-TS).[3][4] References ^ Adis Insight drug profile: Pexidartinib ^ Microglial Magic: Drug Wipes Them Out, New Set Appears (PLX3397) ^ "FDA approves first therapy for rare joint tumor". FDA. 2 August 2...

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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/Pexidartinib

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Possible Dosages for this and Related Drugs:

Pexidartinib Hydrochloride
  • Capsule: 200mg
Note: Above list includes dosages for all drugs with the same combination of active ingredients.

NDC Database Records for Turalio: (1 result)

Sorted by National Drug Code
  • 65597-402 Turalio 200 mg Oral Capsule by Daiichi Sankyo Inc.

Other drugs which contain Pexidartinib Hydrochloride or a similar ingredient: (1 result)




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