for oral use Initial U.S. Approval: 2017
enasidenib tabletsis an isocitrate dehydrogenase-2 inhibitor indicated for the treatment of adult patients with relapsed or refractory acute myeloid leukemia (AML) with an isocitrate dehydrogenase-2 (IDH2) mutation as detected by an FDAapproved test.
Facts about Enasidenib Tablets
Approval Date: 2017
Proprietary Name: On Request
Active Ingredient(s): Enasidenib Tablets
Dosage Forms And Strengths: Tablets: 50 mg or 100 mg
Current indications: acute myeloid leukemia (AML)
Medicine Approved By: – European Medical Agency (EMA), Food and Drug Administration (FDA), Health Canada, Therapeutic Goods Administration (TGA), Medsafe (NZ)
Summary of FDA approved use on approval date: Click Here
(see Drugs@FDA for complete indication)
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Query For Enasidenib Tablets
Approved accessible "Enasidenib Tablets"
enasidenib tabletsis is a prescription medicine used to treat people with acute myeloid leukemia (AML) with an isocitrate dehydrogenase-2 (IDH2) mutation whose disease has come back or has not improved after previous treatment(s). It is not known if IDHIFA is safe and effective in children. Active ingredient: enasidenib Inactive ingredients: colloidal silicon dioxide, hydroxypropyl cellulose, hypromellose acetate succinate, iron oxide yellow, magnesium stearate, microcrystalline cellulose, polyethylene glycol, polyvinyl alcohol, sodium lauryl sulfate, sodium
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