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 : 2021-10-07
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
A Ivermectin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ivermectin, including repackagers and relabelers. The FDA regulates Ivermectin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ivermectin 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 Ivermectin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ivermectin supplier is an individual or a company that provides Ivermectin active pharmaceutical ingredient (API) or Ivermectin finished formulations upon request. The Ivermectin suppliers may include Ivermectin API manufacturers, exporters, distributors and traders.
click here to find a list of Ivermectin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price 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 Ivermectin Drug Master File in Japan (Ivermectin JDMF) empowers Ivermectin 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 Ivermectin JDMF during the approval evaluation for pharmaceutical products. At the time of Ivermectin 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 Ivermectin suppliers with JDMF on PharmaCompass.
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