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Mylan introduces generic Boniva injection

The US Food and Drug Administration (FDA) had granted clearance for Mylan’s abbreviated new drug application (ANDA) for this product, which is indicated to treat osteoporosis in postmenopausal

FDA approves Merck’s anti-PD-1 therapy Keytruda

The indication of Keytruda 2mg/kg every three weeks is approved under accelerated approval based on tumor response rate and durability of response. Keytruda, the first anti-programmed death receptor-1