STADA

STADA

approved_indications Approved Foreign Follow-On Biologics / Biosimilars

Biosimilars Approved In The E.U.

Libmyris / Hukyndra (high-concentration adalimumab) (Stada Arzneimittel AG / Alvotech) (November-2021)Movymia (teriparatide) (STADA Arzneimittel) (January-2017)Oyavas (bevacizumab) (STADA) (March-2021)Silapo (epoetin zeta) (STADA) (December-2007)Silapo (epoetin zeta) (STADA) (December-2007)Uzpruvo® (ustekinumab) (Alvotech / STADA Arzneimittel) (January-2024)Ximluci® (ranibizumab) (STADA / Xbrane) (November-2022 in the EU; January-2023 in the United Kingdom)

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Methodology

Information contained in the Venable BiologicsHQ database relates to FDA-approved drug products listed in the CDER Purple Book or on the FDA website (www.fda.gov). Information relating to FDA licensed products, FDA-approved indications, and aBLA and 505(b)(2) applications is obtained from public sources including the U.S. FDA website (www.fda.gov). Information relating to litigations is given only for cases active from January 31, 2010 onward. Information relating to foreign biosimilar / biologics follow-on products approved in Australia, Canada, the E.U., Japan and South Korea is from public sources. Statistics graphics are compiled from information contained in the Venable BiologicsHQ database.

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