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🇪🇺EU · EMAWithdrawnATC: L01XE02

Gefitinib Mylan(gefitinib)

Carcinoma, Non-Small-Cell Lung

Marketing Authorisation Holder: Mylan Pharmaceuticals Limited

EMA Authorisation: 27/09/2018

INN: gefitinib

Indication

Gefitinib Mylan is indicated as monotherapy for the treatment of adult patients with locally advanced or metastatic non small cell lung cancer (NSCLC) with activating mutations of EGFR TK.

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.