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Ammonul FDA Approval History

FDA Approved: Yes (First approved February 17, 2005)
Brand name: Ammonul
Generic name: sodium benzoate and sodium phenylacetate
Dosage form: Injection
Company: Medicis
Treatment for: Hyperammonemia

Ammonul (sodium benzoate and sodium phenylacetate) is indicated as an adjunctive therapy for the treatment of acute hyperammonemia and associated encephalopathy in patients with deficiencies in enzymes of the urea cycle.

Development timeline for Ammonul

Feb 17, 2005Approval Ammonul Medicis - Treatment for Urea Cycle Disorder

Further information

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