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Regulatory milestone expands Teva's specialty product line, signaling potential revenue growth and improved mix; actual stock impact depends on launch success, payer coverage, and market uptake.
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Teva received FDA approval for Weltruza extended-release injectable suspension, the first and only once-monthly subcutaneous olanzapine for adults with schizophrenia. This milestone diversifies Teva's specialty portfolio beyond generics and may drive growth; payer coverage and uptake will determine the near-term stock impact.
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