FDA Approves L-glutamine Powder for the Treatment of Sickle Cell Disease

Jul 06

2017

The U.S. Food and Drug Administration approved L-glutamine oral powder (Endari™, Emmaus Medical, Inc.) for oral administration to reduce the acute complications of sickle cell disease in adult and pediatric patients 5 years and older.

Citations

APA

American Society of Hematology. (2017).
FDA Approves L-glutamine Powder for the Treatment of Sickle Cell Disease.
Retrieved from https://www.hematology.org/education/clinicians/drug-resources/fda-alerts/2017/fda-approves-l-glutamine-powder-for-the-treatment-of-sickle-cell-disease.

Chicago

American Society of Hematology.
"FDA Approves L-glutamine Powder for the Treatment of Sickle Cell Disease." Hematology.org.
https://www.hematology.org/education/clinicians/drug-resources/fda-alerts/2017/fda-approves-l-glutamine-powder-for-the-treatment-of-sickle-cell-disease
(label-accessed December 12, 2024).

MLA

"American Society of Hematology."
FDA Approves L-glutamine Powder for the Treatment of Sickle Cell Disease, 12 Dec. 2024 ,
https://www.hematology.org/education/clinicians/drug-resources/fda-alerts/2017/fda-approves-l-glutamine-powder-for-the-treatment-of-sickle-cell-disease.

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