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🇪🇺EU · EMAAuthorisedATC: L02BA03

Fulvestrant Mylan(fulvestrant)

Breast Neoplasms

Marketing Authorisation Holder: Mylan Pharmaceuticals Limited

EMA Authorisation: 08/01/2018

INN: fulvestrant

Indication

Fulvestrant is indicated for the treatment of estrogen receptor positive, locally advanced or metastatic breast cancer in postmenopausal women: not previously treated with endocrine therapy, or with disease relapse on or after adjuvant anti-estrogen therapy, or disease progression on antiestrogen therapy.

Official EMA Resources

View on EMA (ema.europa.eu)

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Medical disclaimer: This information is intended for qualified healthcare professionals. Always verify with the official EMA Summary of Product Characteristics (SmPC) before clinical use.