Levamisole
CAS number: 14769-73-4
Molecular formula: C11H12N2S
molecular weight: 204.291
Chemical structure:
Producers shown on SFDA
(Record date:08/09/2021)
Producer | Documents | GMP Valid till(based on SFDA) |
Henan Houyi Pharmaceutical Co., Ltd. | GMP | Valid till July 2026 |
Changzhou Yabang-QH Pharmachem Co., Ltd. | GMP | Valid till December 2025 |
Jiangsu Tianhe Pharmaceutical Co., Ltd. | GMP | Valid till November 2025 |
Henan Huijin Pharmaceutical Co., Ltd. | GMP | Valid till July 2025 |
Lianyungang City Yahui Pharmachem Co., Ltd. | GMP | Valid till June 2024 |
Shaanxi Hanjiang Pharmaceutical Group Co., Ltd. | GMP | Valid till June 2023 |
Producers shown on EP
(Quoted from EP website;record date:08/09/2021)
Substance | Certificate Holder | Certificate Number | Issue Date | Status | End date | Type |
Levamisole Hydrochloride | Shaanxi Hanjiang Pharmaceutical Group Co., Ltd. CN 723 000 Hanzhong City | R1-CEP 1998-095-Rev 01 | 18/09/2009 | VALID | / | Chemistry |
Levamisole Hydrochloride | NANJING WHITE WHALE PHARMACEUTICAL CO., LTD. CN 210 047 Nanjing City | R1-CEP 2013-154-Rev 00 | 02/09/2019 | VALID | / | Chemistry |
Producer:Henan Houyi Pharmaceutical Co., Ltd. is subordinate to Henan Houyi industrial group. The company covers an area of 800 mu, with a fermentation tonnage of 4000 tons and a synthesis capacity of 13800 tons. After completion, it will be a large production base of veterinary API in the Central Plains.
The company's main product production line has passed GMP acceptance, and the annual sales of sulfamethoxam and Cyclopropylamine are 500 tons and 1000 tons respectively; After tylosin and acetylisovaleryl tylosin are launched, the annual output can reach 500 tons and 200 tons.
Registered capital:RMB 128 million
Producer:Changzhou Yabang-QH Pharmachem Co., Ltd.is subordinate to Jiangsu Qihui Pharmaceutical Technology Co., Ltd. the company's quality system has passed who certification, EU EDQM certification and US FDA certification, and obtained eu-gmp certificate. Most products have been registered with asmfs and CEPS in Europe, and some products vmfs have passed US FDA certification. EHS system has obtained the effective certification of ISO14001 environmental management system and OHSAS18001 occupational safety and health management system since 2007.
Staff size:200-299 persons
Registered capital:RMB 50 million
Producer:Jiangsu Tianhe was founded in 2007. The company covers an area of 100000 square meters, with 18600 square meters of production workshop, 3000 square meters of clean area production workshop and 2000 square meters of testing center and R & D center. It has 8 GMP production lines, of which 3 are multi-functional production lines, which can undertake the processing, production and verification of kilogram ton API.
Staff size:100-199 persons
Registered capital:RMB 99.9 million
Producer:Henan Huijin Pharmaceutical Co., Ltd. covers an area of 200 mu with a total investment of 100 million yuan. The company has an engineering technology research center and more than a dozen API synthesis workshops with an annual production capacity of 1000 tons.
Staff size:/
Registered capital:RMB 10 million
Producer:Lianyungang City Yahui Pharmachem Co., Ltd. is subordinate to Jiangsu Qihui Pharmaceutical Technology Co., Ltd. the company's quality system has passed who certification, EU EDQM certification and US FDA certification, and obtained eu-gmp certificate. Most products have been registered with asmfs and CEPS in Europe, and some products vmfs have passed US FDA certification. EHS system has obtained the effective certification of ISO14001 environmental management system and OHSAS18001 occupational safety and health management system since 2007, and has passed the safety, environmental protection and social responsibility audit of well-known pharmaceutical enterprises and third-party institutions at home and abroad for many times.
Staff size:About 50 persons
Registered capital:RMB 20 million
Producer:Shaanxi Hanjiang Pharmaceutical Group Co., Ltd. currently has four API production workshops and two pharmaceutical intermediate workshops that meet GMP specifications. In recent years, the company has successively passed the new GMP audit of CFDA, the GMP audit of the Ministry of agriculture of the people's Republic of China, the FDA of the United States, the EDQM of the European Union (EU) and the official GMP audit of Mexico. All raw materials have obtained the written GMP confirmation letter for export to the EU issued by China CFDA. In terms of quality management and EHS, the company has successively passed the certification of ISO9001, ISO14001 and OHSMS18001 systems.
Staff size:600-699 persons
Registered capital:RMB139 million
For supply and market information, please feel free to contact Mr. Paul, paulzhang@yinuopharmchem.com, WhatsApp: +8618402846978