Shilpa Medicare gets US FDA nod for its ANDA, Erlotinib tablets

| Updated on November 06, 2019

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Shilpa Medicare Ltd has received the US Food and Drug Administration final approval for its ANDA, Erlotinib Tablets, 25 mg, 100 mg, and 150 mg on Tuesday. Erlotinib Tablets, a generic equivalent of reference listed drug Tarceva, used in the treatment of patients with metastatic non-small cell lung cancer and locally advanced, unresectable or metastatic pancreatic cancer as recommended in the label approved by FDA.

According to IQVIA MAT Q2 2019 data, the US market for Erlotinib Tablets is approximately $172 million. The stock of Shilpa Medicare closed flat at ₹310 on the BSE.

Published on November 07, 2019

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