01 1Zhejiang Hisun Pharmaceutical Co., Ltd.
01 1Ace Biopharm Co., Ltd.
01 1Ivermectin
01 1China
Registrant Name : Ace Biopharm Co., Ltd.
Registration Date : 2025-02-21
Registration Number : 20250221-211-J-1776
Manufacturer Name : Zhejiang Hisun Pharmaceutica...
Manufacturer Address : 56 Binhai Road, Jiaojiang District, Taizhou City, Zhejiang Province, People's Republi...
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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.
In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a Ivomec Drug Master File in Korea (Ivomec KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Ivomec. The MFDS reviews the Ivomec KDMF as part of the drug registration process and uses the information provided in the Ivomec KDMF to evaluate the safety and efficacy of the drug.
After submitting a Ivomec KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their Ivomec API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Ivomec suppliers with KDMF on PharmaCompass.
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