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Zhejiang Jolly Pharmaceutical Co Ltd

Zhejiang Jolly Pharmaceutical Co.,LTD researches, produces, and markets Chinese medicinal products in China and internationally. Its key offerings include Wuling capsules for insomnia and related symptoms, Lingze tablets for benign prostatic hyperplasia and kidney deficiency, Bailing tablets as adjuvant therapy for respiratory conditions, and Linglianhua particles for perimenopausal syndrome. The company also provides injections such as azithromycin, clindamycin phosphate, doxapram, pefloxacin mesylate, adenosine cyclophosphate, and sodium nitroprusside, as well as materials like cephalosporin sinensis, fermented cordyceps, and Wuling powders. It invests in and participates in medical services at Deqing No.3 People's Hospital. Formerly known as Zhejiang Jolly Pharmaceutical Health Products Co., LTD., it changed its name in 1998, was founded in 1995, and is based in Huzhou, China.

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300181.CS

Zhejiang Jolly Pharmaceutical's Linglianhua Granules Receive Clinical Trial Approval, Planned New Indication for Perimenopausal Anxiety

Zhejiang Jolly Pharmaceutical Co., Ltd. announced on August 12 that its marketed product Linglianhua Granules has received a Drug Clinical Trial Approval Notice issued by the National Medical Products Administration, agreeing to conduct clinical trial research for a new functional indication. The proposed new indication is perimenopausal syndrome with anxiety state of heart-kidney disharmony pattern. The product's registration classification is Category 2.3 of traditional Chinese medicine, with acceptance number CXZL2600050. Linglianhua Granules is one of the company's Wuling series products and is an exclusive over-the-counter product in China. It uses Wuling fungal powder as the core raw material, combined with Chinese medicinal materials such as glossy privet fruit, thinleaf milkwort root, and yerbadetajo herb. It was originally used for perimenopausal syndrome of heart-kidney disharmony pattern. The company stated that after this approval, it will organize and carry out clinical trials. Due to the long cycle, multiple stages, and high risks of drug research and development, this matter will not have a significant impact on performance, and there is uncertainty in subsequent clinical trials and market launch.
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