Lupin Limited announced on December 1 that it received FDA approval for its biosimilar product, ARMLUPEG (pegfilgrastim-unne). ARMLUPEG is approved as a 6 mg/0.6 mL single-dose prefilled syringe presentation, referencing Amgen’s NEULASTA. ARMLUPEG is indicated to decrease the incidence of febrile neutropenia in patients with non-myeloid malignancies who are receiving…
