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Henan Newland Pharmaceutical Co. Ltd. A

Newland Pharmaceutical Co., Ltd. researches, develops, produces, and sells pharmaceutical intermediates and APIs in China. Its intermediates include L-4-hydroxyphenylglycine methyl ester, L-hydroxyphenylglycine potassium salt, L-4-hydroxyphenylglycine, and p-toluenesulfonic acid. Its APIs include ropivacaine hydrochloride, naphazoline hydrochloride, moxifloxacin hydrochloride, lidocaine hydrochloride, vildagliptin, tadalafil, chlorpheniramine maleate, clopidogrel bisulfate, lidocaine, gatifloxacin, febuxostat, esomeprazole sodium, and esomeprazole magnesium. Formerly Henan Newland Pharmaceutical Co., Ltd., it changed its name to Newland Pharmaceutical Co., Ltd. in June 2023. Founded in 2005, the company is based in Changge, China.

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301277.CS

Xintiandi's first-half net profit attributable to parent was 60.77 million yuan, down 22.1% year on year

Xintiandi released its 2026 interim report. First-half net profit attributable to the parent was 60.77 million yuan, down 22.1% year on year, while operating revenue was 397 million yuan, up 10.6% year on year. Net profit attributable to the parent after deducting non-recurring items was 54.72 million yuan, down 23.8% year on year. Net operating cash flow was 6.98 million yuan, down 79.0% year on year. Earnings per share were 0.155 yuan. In the second quarter, operating revenue was 190 million yuan, up 36.7% year on year, and net profit attributable to the parent was 24.67 million yuan, up 14.9% year on year. As of the end of the second quarter, total assets were 1.754 billion yuan, down 1.4% from the end of the previous year, and net assets attributable to the parent were 1.534 billion yuan, down 1.1% from the end of the previous year. The company said its main business has not undergone major changes, and it is implementing a new strategy-driven development model to build a modern platform-based company. In the pharmaceutical intermediates business, the main products are the levophenylglycine series and the p-toluenesulfonic acid series. In the active pharmaceutical ingredients business, 15 products have been approved for registration in China, and the formulations business is also advancing integrated development.
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301277.CS

Newland Pharmaceutical's Amlodipine Besylate API Receives Marketing Approval

Newland Pharmaceutical Co., Ltd. announced that on July 21, 2026, it received the Chemical Active Pharmaceutical Ingredient Marketing Application Approval Notification for amlodipine besylate API from the National Medical Products Administration. The registration number is Y20240001499, valid until July 20, 2031, and the status displayed on the CDE raw and auxiliary materials registration information platform is A. Amlodipine besylate is a long-acting calcium channel blocker used to treat hypertension, coronary heart disease, chronic stable angina, and vasospastic angina. The company stated that this approval will further enrich its product portfolio and enhance market competitiveness, while noting that pharmaceutical production and sales are subject to market conditions and other factors, involving a degree of uncertainty.
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