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Teva receives European Commission approvals for PONLIMSI® (denosumab) Biosimilar to Prolia® and DEGEVMA® (denosumab) Biosimilar to Xgeva®

Teva Pharmaceutical Industries Limited American Depositary Shares  (TEVA) 
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US:NYSE Investor Relations: ir.tevapharm.com
PDF Following the positive opinions of the Committee for Medicinal Products for Human Use (CHMP), the European Commission has granted marketing authorizations for Teva’s bio [Read more]