SSY Group Ltd. Receives Regulatory Approval from China's NMPA for Allopurinol Tablets Production

Reuters

09/01

SSY Group Ltd. Receives Regulatory Approval from China's NMPA for Allopurinol Tablets Production

SSY Group Ltd. has announced that it has received regulatory approval from the National Medical Products Administration of China (NMPA) for the production and registration of Allopurinol Tablets (0.1g). This approval classifies it as a type 3 chemical drug and confirms its compliance with the consistency evaluation. The Allopurinol Tablets are intended for patients with primary or secondary gout, as well as for those undergoing treatment for leukemia, lymphoma, and malignant tumors, and for the treatment of recurrent calcium oxalate stones. This development marks a significant step in the company's product offerings, following the prior approval of Allopurinol bulk drug registration for market preparations. This announcement serves to update shareholders and potential investors on the company's latest business progress.

Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. SSY Group Ltd. published the original content used to generate this news brief on September 01, 2025, and is solely responsible for the information contained therein.

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Receives Regulatory Approval from China's NMPA for Allopurinol Tablets Production","media":"Reuters","content":"<html xmlns=\"http://www.w3.org/1999/xhtml\" xmlns:newsg2=\"http://iptc.org/std/nar/2006-10-01/\" xmlns:xhtml=\"http://www.w3.org/1999/xhtml\"><head><title>\n      SSY Group Ltd. Receives Regulatory Approval from China's NMPA for Allopurinol Tablets Production\n    </title></head><body><div xmlns:xsd=\"http://www.w3.org/2001/XMLSchema\" xmlns:xsi=\"http://www.w3.org/2001/XMLSchema-instance\">\n<p>\n        SSY Group Ltd. has announced that it has received regulatory approval from the National Medical Products Administration of China (NMPA) for the production and registration of Allopurinol Tablets (0.1g). This approval classifies it as a type 3 chemical drug and confirms its compliance with the consistency evaluation. 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Receives Regulatory Approval from China's NMPA for Allopurinol Tablets Production\n</h2>\n<h4 class=\"meta\">\n<a class=\"head\" href=\"https://laohu8.com/wemedia/1032215980\">\n\n<div class=\"h-thumb\" style=\"background-image:url(https://community-static.tradeup.com/news/4567337cbdf294b657b1fa87c5488b48);background-size:cover;\"></div>\n\n<div class=\"h-content\">\n<p class=\"h-name\">Reuters </p>\n<p class=\"h-time smaller\">2025-09-01 16:38</p>\n</div>\n</a>\n</h4>\n</header>\n<article>\n<html xmlns=\"http://www.w3.org/1999/xhtml\" xmlns:newsg2=\"http://iptc.org/std/nar/2006-10-01/\" xmlns:xhtml=\"http://www.w3.org/1999/xhtml\"><head><title>\n      SSY Group Ltd. Receives Regulatory Approval from China's NMPA for Allopurinol Tablets Production\n    </title></head><body><div xmlns:xsd=\"http://www.w3.org/2001/XMLSchema\" xmlns:xsi=\"http://www.w3.org/2001/XMLSchema-instance\">\n<p>\n        SSY Group Ltd. has announced that it has received regulatory approval from the National Medical Products Administration of China (NMPA) for the production and registration of Allopurinol Tablets (0.1g). This approval classifies it as a type 3 chemical drug and confirms its compliance with the consistency evaluation. The Allopurinol Tablets are intended for patients with primary or secondary gout, as well as for those undergoing treatment for leukemia, lymphoma, and malignant tumors, and for the treatment of recurrent calcium oxalate stones. This development marks a significant step in the company's product offerings, following the prior approval of Allopurinol bulk drug registration for market preparations. 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