01 2Hovione PharmaScience Limited
02 1Zhejiang Hisun Pharmaceutical Co. , Ltd.
01 3Ivermectin
01 1China
02 2Portugal
Registration Number : 304MF10006
Registrant's Address : Estrada Coronel Nicolau de Mesquita Taipa, Macau S. A. R. China
Initial Date of Registration : 2022-01-11
Latest Date of Registration : 2022-01-11
Registration Number : 221MF10281
Registrant's Address : Estrada Coronel Nicolau de Mesquita Taipa, Macau S. A. R. China
Initial Date of Registration : 2009-12-18
Latest Date of Registration : 2025-08-21
Registration Number : 304MF10048
Registrant's Address : 46 Waisha Road, Jiaojiang District, Taizhou City, Zhejiang Province, P. R. China 3180...
Initial Date of Registration : 2022-03-02
Latest Date of Registration : 2022-03-02
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PharmaCompass offers a list of Ivermectin API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Ivermectin manufacturer or Ivermectin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Ivermectin manufacturer or Ivermectin supplier.
A Ivomec manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ivomec, including repackagers and relabelers. The FDA regulates Ivomec manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ivomec API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Ivomec manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Ivomec supplier is an individual or a company that provides Ivomec active pharmaceutical ingredient (API) or Ivomec finished formulations upon request. The Ivomec suppliers may include Ivomec API manufacturers, exporters, distributors and traders.
click here to find a list of Ivomec suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The Ivomec Drug Master File in Japan (Ivomec JDMF) empowers Ivomec API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the Ivomec JDMF during the approval evaluation for pharmaceutical products. At the time of Ivomec JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Ivomec suppliers with JDMF on PharmaCompass.
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