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FUSEN PHARM

0.800

+0.0405.26%

Volume:67.00K

Turnover:50.65K

Market Cap:591.20M

PE:-2.83

High:0.800

Open:0.760

Low:0.740

Close:0.760

52wk High:1.750

52wk Low:0.235

Shares:739.00M

HK Float Shares:739.00M

Volume Ratio:2.37

T/O Rate:0.01%

Dividend:- -

Dividend Rate:- -

EPS(LYR):-0.283

ROE:-40.49%

ROA:-2.47%

PB:1.54

PE(LYR):-2.83

PS:2.21

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Overview Company News Filings

FUSEN PHARM (01652) Appoints Zhongzheng Tianheng as New Auditor

Fusen Pharmaceutical Replaces Auditor After Fee Dispute

FUSEN PHARM (01652): "Nicardipine Hydrochloride Injection" Generic Drug Application Approved for Market Launch

Fusen Pharmaceutical - Approval Issued by Nmpa for Consistency Evaluation of Nicardipine Hydrochloride Injection

THOMSON REUTERS

Fusen Pharmaceutical Wins Regulatory Approval for Nicardipine Hydrochloride Injection in China

Fusen Pharmaceutical (01652) Releases Monthly Return for November 2025

Bulletin Express

HK Stock Movement | FUSEN PHARM (01652) Surges Over 7% as Its "Azilsartan Potassium Tablets" Gain Market Approval

Fusen Pharmaceutical's Unit Get China Nod for Marketing of Hypertension Drug

MT Newswires Live

Fusen Pharmaceutical - Approval From Nmpa

THOMSON REUTERS

Fusen Pharmaceutical Co Ltd - Measartan Potassium Tablets Approved for Marketing

THOMSON REUTERS

Further weakness as Fusen Pharmaceutical (HKG:1652) drops 12% this week, taking five-year losses to 85%

Simply Wall St.

Fusen Pharmaceutical (01652) Reports October 2025 Monthly Securities Movements

Bulletin Express

HK Stock Movement | FUSEN PHARM (01652) Surges Nearly 74% Intraday as Enzalutamide Soft Capsule Approved and Metformin Empagliflozin Tablet Included in National Bulk-Buy Program

FUSEN PHARM (01652): "Enzalutamide Soft Capsule" Approved for Market Launch

Fusen Pharmaceutical Wins Approval for Enzalutamide Soft Capsules in China

BRIEF-Fusen Pharmaceutical Says Enzalutamide Soft Capsules Approved For Marketing by NMPA

Fusen Pharmaceutical Co Ltd - Enzalutamide Soft Capsules Approved for Marketing

THOMSON REUTERS

Fusen Pharmaceutical - Approval From China's National Medical Products Administration

THOMSON REUTERS

Fusen Pharmaceutical (1652) Announces Selection in Eleventh Batch of National Centralised Medicines Procurement

Bulletin Express

FUSEN PHARM (01652): Metformin Empagliflozin Tablets (I) Shortlisted in China's 11th National Drug Centralized Procurement Bidding

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group's...","market":"fut","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":"","theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"0","news_top_title":null,"news_tag":"executive","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["BK1191","01652"],"gpt_icon":0},{"id":"2593747826","title":"Fusen Pharmaceutical Replaces Auditor After Fee Dispute","url":"https://stock-news.laohu8.com/highlight/detail?id=2593747826","media":"Reuters","labels":["event"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2593747826?lang=en_us&edition=fundamental","pubTime":"2025-12-24 17:04","pubTimestamp":1766567041,"startTime":"0","endTime":"0","summary":"Fusen Pharmaceutical Company Ltd. announced a change of auditor after KPMG resigned from its role effective 24 December 2025, citing an inability to reach a consensus on the proposed audit fee for the company's 2025 consolidated financial statements. The company stated there was no disagreement with KPMG aside from the fee issue, and no other matters needed to be brought to shareholders' attention. CCTH CPA Limited has been appointed as the new auditor. The board believes this change will not materially affect the company's annual audit or the release of its annual results for 2025.Disclaimer: This news brief was created by Public Technologies  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. Fusen Pharmaceutical Company Ltd. published the original content used to generate this news brief via IIS, t","market":"nz","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://api.refinitiv.com/data/news/v1/stories/urn:newsml:reuters.com:20251224:nNDL8CpqD6:1","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"0","news_top_title":null,"news_tag":"event","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["01652","BK1191"],"gpt_icon":0},{"id":"1184071340","title":"FUSEN PHARM (01652): \"Nicardipine Hydrochloride Injection\" Generic Drug Application Approved for Market Launch","url":"https://stock-news.laohu8.com/highlight/detail?id=1184071340","media":"Stock News","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1184071340?lang=en_us&edition=fundamental","pubTime":"2025-12-12 20:50","pubTimestamp":1765543822,"startTime":"0","endTime":"0","summary":"FUSEN PHARM (01652) announced that its wholly-owned subsidiary, Henan FUSEN PHARM, has received approval from China's National Medical Products Administration for the generic drug application of...","market":"fut","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":"","theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"productRelease","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["BK1191","01652"],"gpt_icon":0},{"id":"2590506147","title":"Fusen Pharmaceutical -  Approval Issued by Nmpa for Consistency Evaluation of Nicardipine Hydrochloride Injection","url":"https://stock-news.laohu8.com/highlight/detail?id=2590506147","media":"THOMSON REUTERS","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2590506147?lang=en_us&edition=fundamental","pubTime":"2025-12-12 20:42","pubTimestamp":1765543369,"startTime":"0","endTime":"0","summary":null,"market":"fut","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://api.refinitiv.com/data/news/v1/stories/urn:newsml:reuters.com:20251212:nFWN3XH1GR:1","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"0","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":"reuters_en_live","symbols":["BK1191","01652"],"gpt_icon":0},{"id":"2590506164","title":"Fusen Pharmaceutical Wins Regulatory Approval for Nicardipine Hydrochloride Injection in China","url":"https://stock-news.laohu8.com/highlight/detail?id=2590506164","media":"Reuters","labels":["policyRegulatory"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2590506164?lang=en_us&edition=fundamental","pubTime":"2025-12-12 20:41","pubTimestamp":1765543309,"startTime":"0","endTime":"0","summary":"Fusen Pharmaceutical Company Limited has announced that it has received regulatory approval from the National Medical Products Administration of the PRC for the consistency evaluation of its Nicardipine Hydrochloride Injection. Developed by its wholly-owned subsidiary, Henan Fusen Pharmaceutical Company Limited, this product is intended for the emergency management of perioperative hypertension and hypertensive emergencies. The approval covers multiple specifications, including 2ml:2mg, 5ml:5mg, and 10ml:10mg, making Fusen one of the companies in China with the most comprehensive range of this product. No grant or funding from multiple organizations was mentioned.Disclaimer: This news brief was created by Public Technologies  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. 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The announcement shows that the company’s total authorized share capital remained at...","market":"us","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":"","theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"0","news_top_title":null,"news_tag":"dataReport,SGX","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["01652"],"gpt_icon":0},{"id":"1131439795","title":"HK Stock Movement | FUSEN PHARM (01652) Surges Over 7% as Its \"Azilsartan Potassium Tablets\" Gain Market Approval","url":"https://stock-news.laohu8.com/highlight/detail?id=1131439795","media":"Stock News","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1131439795?lang=en_us&edition=fundamental","pubTime":"2025-11-17 13:38","pubTimestamp":1763357894,"startTime":"0","endTime":"0","summary":"FUSEN PHARM (01652) rose more than 7%, reaching HK$0.88 by the time of writing, with a trading volume of HK$1.264 million. The surge follows the company's announcement on November 14 that its...","market":"other","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":"","theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"productRelease","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["01652","BK1191"],"gpt_icon":0},{"id":"2583357261","title":"Fusen Pharmaceutical's Unit Get China Nod for Marketing of Hypertension Drug","url":"https://stock-news.laohu8.com/highlight/detail?id=2583357261","media":"MT Newswires Live","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2583357261?lang=en_us&edition=fundamental","pubTime":"2025-11-14 18:28","pubTimestamp":1763116120,"startTime":"0","endTime":"0","summary":"Fusen Pharmaceutical  said China's National Medical Products Administration approved Measartan Potassium Tablets for marketing, a Friday Hong Kong bourse filing said.The drug, developed by unit Jiaheng  Pharmaceutical Technology is used for the treatment of primary hypertension.","market":"fut","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://www.mtnewswires.com/","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"productRelease","news_rank":0,"length":0,"strategy_id":0,"source":"mtnewswires_news","symbols":["01652","BK1191"],"gpt_icon":0},{"id":"2583734125","title":"Fusen Pharmaceutical - 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Authorized share capital remained at HKD 20,000,000, comprising...","market":"hk","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":"","theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"0","news_top_title":null,"news_tag":"SGX","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["01652"],"gpt_icon":0},{"id":"1177679917","title":"HK Stock Movement | FUSEN PHARM (01652) Surges Nearly 74% Intraday as Enzalutamide Soft Capsule Approved and Metformin Empagliflozin Tablet Included in National Bulk-Buy Program","url":"https://stock-news.laohu8.com/highlight/detail?id=1177679917","media":"Stock News","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1177679917?lang=en_us&edition=fundamental","pubTime":"2025-10-31 10:34","pubTimestamp":1761878056,"startTime":"0","endTime":"0","summary":"FUSEN PHARM (01652) surged nearly 74% intraday, and as of the latest update, the stock was up 49.28% at HKD 1.03, with a turnover of HKD 10.37 million. The company announced that its wholly-owned...","market":"hk","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":"","theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"2","news_top_title":null,"news_tag":"productRelease","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["BK1191","01652"],"gpt_icon":0},{"id":"1139826453","title":"FUSEN PHARM (01652): \"Enzalutamide Soft Capsule\" Approved for Market Launch","url":"https://stock-news.laohu8.com/highlight/detail?id=1139826453","media":"Stock News","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1139826453?lang=en_us&edition=fundamental","pubTime":"2025-10-30 22:02","pubTimestamp":1761832936,"startTime":"0","endTime":"0","summary":"FUSEN PHARM (01652) announced that its wholly-owned subsidiary, Jiaheng (Zhuhai Hengqin) Pharmaceutical Technology Co., Ltd., has received approval from China's National Medical Products...","market":"sh","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":"","theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["BK1191","01652"],"gpt_icon":0},{"id":"2579128347","title":"Fusen Pharmaceutical Wins Approval for Enzalutamide Soft Capsules in China","url":"https://stock-news.laohu8.com/highlight/detail?id=2579128347","media":"Reuters","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2579128347?lang=en_us&edition=fundamental","pubTime":"2025-10-30 21:49","pubTimestamp":1761832193,"startTime":"0","endTime":"0","summary":"Fusen Pharmaceutical Company Ltd. has announced that its wholly-owned subsidiary, Jiaheng  Pharmaceutical Technology Company Limited, has received marketing approval from the National Medical Products Administration of the People's Republic of China for its Enzalutamide Soft Capsules. This approval covers the treatment of adult patients with non-metastatic castration-resistant prostate cancer  at high risk of metastasis, as well as adult patients with metastatic castration-resistant prostate cancer  who have mild or no symptoms after unsuccessful androgen deprivation therapy and who have not received chemotherapy. The company highlights that the product demonstrates quality and efficacy consistent with the original reference drug and offers a favorable risk-benefit ratio for patients. No other organizations are mentioned as recipients of this regulatory approval.Disclaimer: This news brief was created by Public Technologies  using generative artificial intelligence. 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