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Alembic gets FDA tentative approval for generic Bosutinib to treat certain leukemia patients.
Alembic Pharmaceuticals has received tentative FDA approval for its 400 mg generic Bosutinib tablets, used to treat adult patients with Philadelphia chromosome-positive chronic myelogenous leukemia, including those newly diagnosed or resistant to prior therapies.
The approval, via a supplemental ANDA, confirms therapeutic equivalence to the brand-name drug Bosulif.
This follows earlier approvals for 100 mg and 500 mg strengths.
Market entry is pending resolution of patent or exclusivity issues.
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Alembic obtiene la aprobación provisional de la FDA para el Bosutinib genérico para tratar a ciertos pacientes con leucemia.