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, sold under the brand name Turalio, is a kinase inhibitor drug for the treatment of adults with symptomatic tenosynovial giant cell tumor (TGCT) associated with severe morbidity or functional limitations and not amenable to improvement with surgery.[1][2][3][4] Common side effects are increased lactate dehydrogenase (proteins that helps produce energy in the body), increased aspartate aminotransferase (enzymes that ...

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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:

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)

• PEXIDARTINIB