China SXT Pharmaceuticals, Inc. Adds Newly Developed Kuihuapan and Zhudanfen Advanced TCMP Products, and Announces the Expected Continuous Growth of Its Production Capacity of Luxuejin
China SXT Pharmaceuticals (NASDAQ: SXTC) announced the development of Kuihuapan and Zhudanfen, two new Advanced TCMP products, aimed at enhancing its market presence. The annual output is anticipated to reach 300,000 bottles, generating sales of approximately RMB 5 million by March 31, 2023. The company is also focusing on increasing production capacity for its Luxuejin product, expecting sales of over RMB 3 million for the fiscal year ending March 31, 2022. The development leverages Chinese Pharmacopoeia standards to improve clinical effectiveness while meeting rising market demand.
- Development of Kuihuapan and Zhudanfen Advanced TCMP products.
- Expected sales of RMB 5 million from new products by March 31, 2023.
- Expected sales of over RMB 3 million for Luxuejin by March 31, 2022.
- Increase in production capacity for Luxuejin due to rising market demand.
- None.
TAIZHOU, China, Jan. 14, 2022 /PRNewswire/ -- China SXT Pharmaceuticals, Inc. (NASDAQ: SXTC) ("China SXT" or the "Company"), a specialty pharmaceutical company focusing on the research, development, manufacturing, marketing, and sales of Traditional Chinese Medicine Pieces ("TCMPs"), including Advanced TCMPs (Directly-Oral TCMP and After-Soaking-Oral TCMP), fine TCMPs, regular TCMPs, and TCM Homologous Supplements ("TCMHS") announced today that it develops and commercializes the Kuihuapan After-Soaking-Oral TCMP and Zhudanfen Directly-Oral TCMP products. The Kuihuapan products are produced according to the four processing specifications of Chinese Pharmacopoeia (2020 Edition) No. 34 of China Heilongjiang food and Drug Administration Note Letter [2020], and have the functions of clearing heat, calming liver, dredging collaterals and relieving pain. Its indications include dizziness, tinnitus, joint pain, hyperuricemia, gout, hypertension and other symptoms. The Zhudanfen products are produced according to the processing specifications of Chinese Pharmacopoeia (2020 Edition), it has the functions of clearing heat and moistening dryness, relieving cough and asthma, and detoxifying, and is suitable for sudden cough, asthma, fever, thirst, red eyes, throat obstruction, jaundice, diarrhea, dysentery, constipation, sores, carbuncle, swelling and poison. Zhudanfen is also listed in the National Medical Insurance Catalogue (No. 697 of the National Medical Insurance Catalogue). We expect that the annual output of both Kuihuapan and Zhudanfen to reach 300,000 bottles, and achieve the sales of about RMB 5 million during the fiscal year ending March 31, 2023.
In addition, although the GMP compliance inspection conducted by Jiangsu Province Medical Products Administration (JSMPA) for the Company's new lyophilization production facilities in June 18, 2021 delayed the production cycle and the production capacity decreased consequently, compared with the same period. JSMPA completed its inspection in June 20, 2021. As of December 31, 2021, there are 12 batches of Luxuejin Directly-Oral TCMP products produced by lyophilization process. The Company has consumed 2.08 tons of fresh bloods of Cuerus Nippon as the raw materials, and the total amount of Luxuejin after freeze-drying is 316.92 kilogram, which is expected to achieve the sales of more than RMB 3 million during the fiscal year ending March 31, 2022. With the continuous increased market demand for Luxuejin, we will work to increase our production capacity and we believe the output value will grow rapidly.
According to the definition of Directly-Oral TCMP and the preclinical research and development strategies of new medicine of FDA and CFDA, our R&D Department chose the standards under the "processing" and "usage" parts of the corresponding TCMPs in the Chinese Pharmacopoeia (2015 Edition), and applies the latest technology and analysis methods to systematically invent a new type of Directly-Oral TCMP product which can be directly taken orally or infused without decoction, and maintains all the original effective components. Thus, it improves clinical curative effects, saves medicinal materials, is easy to carry, and can be stored easily. After-Soaking-Oral TCMP products are another new type of Advanced TCMP that can be brewed in boiling water (similar to tea drinking method), which first appeared in part 4 of Chinese Pharmacopoeia (2015 Edition). Its research and development method is similar to that of Directly-Oral TCMP, and our R&D Department systematically developed a new product series of After-Soaking-Oral TCMP according to the characteristics of its which can be directly brewed with boiling water (or decocted with the traditional TCMP formula), so as to maintain the original effective ingredients to the greatest extent and improve the clinical effects.
"The developed R&D and production of Advanced TCMP products will greatly help us make continuous efforts in leading the R&D of Advanced TCMP and pursuing higher quality products. We believe that this will further expand the market shares of our Directly-Oral TCMP and After-Soaking-Oral TCMP products ", Mr. Feng Zhou, Chief Executive Officer of China SXT, commented.
About China SXT Pharmaceuticals, Inc.
Founded in 2005 and headquartered in Taizhou City, Jiangsu Province, China, China SXT Pharmaceuticals, Inc. is an innovative pharmaceutical company focusing on the research, development, manufacture, marketing and sales of traditional Chinese medicine pieces, which is a type of Traditional Chinese Medicine that has been processed to be ready for use. For more information, please visit www.sxtchina.com
Safe Harbor Statement
This press release contains forward-looking statements as defined by the Private Securities Litigation Reform Act of 1995. Forward-looking statements include statements concerning plans, objectives, goals, strategies, future events or performance, and underlying assumptions and other statements that are other than statements of historical facts. When the Company uses words such as "may, "will, "intend," "should," "believe," "expect," "anticipate," "project," "estimate" or similar expressions that do not relate solely to historical matters, it is making forward-looking statements. Specifically, the Company's statements regarding the closing of the proposed private placement are forward-looking statements. Forward-looking statements are not guarantees of future performance and involve risks and uncertainties that may cause the actual results to differ materially from the Company's expectations discussed in the forward-looking statements. These statements are subject to uncertainties and risks including, but not limited to, the following: the Company's goals and strategies; the Company's future business development; product and service demand and acceptance; changes in technology; the growth of the pharmaceutical market, particularly the Traditional Chinese Medicine Pieces ("TCMPs") market, in China; reputation and brand; the impact of competition and pricing; government regulations; fluctuations in general economic and business conditions in China and the international markets the Company serves and assumptions underlying or related to any of the foregoing and other risks contained in reports filed by the Company with the Securities and Exchange Commission. For these reasons, among others, investors are cautioned not to place undue reliance upon any forward-looking statements in this press release. Additional factors are discussed in the Company's filings with the U.S. Securities and Exchange Commission, which are available for review at www.sec.gov. The Company undertakes no obligation to publicly revise these forward - looking statements to reflect events or circumstances that arise after the date hereof.
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