01 1Huvepharma Italia Srl
02 1Shin Poong Pharmaceutical Co., Ltd.
01 2Shin Poong Pharmaceutical Co., Ltd.
01 2Altesunate
01 1Italy
02 1South Korea
Registrant Name : Shin Poong Pharmaceutical Co., Ltd.
Registration Date : 2021-01-15
Registration Number : Number 1414-8-ND
Manufacturer Name : Huvepharma Italia Srl
Manufacturer Address : Via R. Lepetit, 142 12075 - GARESIO (CN) ITALY
Registrant Name : Shin Poong Pharmaceutical Co., Ltd.
Registration Date : 2011-01-31
Registration Number : 1414-1-ND
Manufacturer Name : Shin Poong Pharmaceutical Co...
Manufacturer Address : 70, Sandan-ro 19beon-gil, Danwon-gu, Ansan-si, Gyeonggi-do
A Artesunate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Artesunate, including repackagers and relabelers. The FDA regulates Artesunate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Artesunate 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 Artesunate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Artesunate supplier is an individual or a company that provides Artesunate active pharmaceutical ingredient (API) or Artesunate finished formulations upon request. The Artesunate suppliers may include Artesunate API manufacturers, exporters, distributors and traders.
click here to find a list of Artesunate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price 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 Artesunate Drug Master File in Korea (Artesunate KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Artesunate. The MFDS reviews the Artesunate KDMF as part of the drug registration process and uses the information provided in the Artesunate KDMF to evaluate the safety and efficacy of the drug.
After submitting a Artesunate 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 Artesunate API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Artesunate suppliers with KDMF on PharmaCompass.
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