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Nexavar is presented as film coated tablets containing 274 mg of sorafenib tosylate, which corresponds to 200 mg of sorafenib, as active substance. Renal cell carcinoma Nexavar is indicated for the treatment of patients with advanced renal cell carcinoma who have failed prior interferon-alpha or interleukin-2 based therapy or are considered unsuitable for such therapy. Reddy’s Laboratories Ltd has launched sorafenib tablets, a therapeutic generic equivalent of Nexavar (sorafenib) in the US market following approval by the US Food and Drug Administration. The product will be launched by NATCO's commercial partner Viatris, a global pharmaceutical company. The German pharmaceutical giant raised €184 million from the sales of Nexavar in the first quarter of 2019 and €712 million in full year 2018. Com Click on any 1 of the 4 Pack Sizes to Add-to-Cart : Brand/Sales Disclaimer: The Brand names and/or Images/Logos as. 2 Discussion on the non-clinical aspects This product is a generic formulation of Nexavar, which is available on the European market.. Natco Pharma will sell 120 tablets for ₹ 8,800 (US0), while still paying a 6% royalty to Bayer Nexavar is presented as film coated tablets containing 274 mg of sorafenib tosylate, which corresponds to 200 mg of sorafenib, as active substance. The FDA has approved Nexavar, or sorafenib, to treat thyroid, liver and kidney cancer Natco Pharma has announced the launch of the first generic version of Nexavar (Sorafenib) tablets in the US market on Wednesday. Several preliminary injunctions issued by Munich Regional Court are in effect until the Federal Patent Court rules on the patent's validity at the end of September. Has a generic version of Nexavar been approved? Helpline: WhatsApp +1 (409)-995-3585 / WeCare@GenuineDrugs123. 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