
Erlotinib® is indicated for:
The treatment of patients with metastatic non-small cell lung cancer (NSCLC) whose tumors have epidermal growth factor receptor (EGFR) exon 19 deletions or exon 21 (L858R) substitution mutations, as confirmed by an FDA-approved test. It may be used as first-line therapy, maintenance therapy, or second-line or later-line therapy following disease progression after at least one prior chemotherapy regimen.
Usage Restrictions:
The safety and effectiveness of Erlotinib in NSCLC patients with other EGFR mutations have not been established.
Concomitant use of Erlotinib with platinum-containing chemotherapy is not recommended.
Erlotinib in combination with gemcitabine is indicated for the first-line treatment of patients with locally advanced, unresectable, or metastatic pancreatic cancer.
FDA,2016.10

Lucius Pharmaceutical Co., Ltd., was established in 2020 in Vientiane, the capital of Laos. It aims to offer safe, effective, and affordable medicines globally. With a factory spanning 25,000 square meters, the company manufactures 200+ generic drugs in diverse therapeutic fields.
Address:No.26 Thongmang village, Xaythany district, Vientiane Capital, Laos
E-mail:laoslucius@gmail.com
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