01 1Hunan Warrant Pharmaceutical Co., Ltd@Dasan Pharmaceutical Co., Ltd
02 1Seongil Bioex Co., Ltd.
01 1Dasan Pharmaceutical Co., Ltd.
02 1Seongil Bioex Co., Ltd.
01 2Coptis chinensis saturated butanol dry extract (4.5~7→1)
01 1China
02 1Blank
Coptis chinensis saturated butanol dry extract (4.5~7→1)
Registrant Name : Dasan Pharmaceutical Co., Ltd.
Registration Date : 2020-04-02
Registration Number : 20200402-12-K-52-02
Manufacturer Name : Hunan Warrant Pharmaceutical...
Manufacturer Address : Jiankang South Road No.5, Liuyang Biomedical Park, Hunan Province, China@342 Deokamsa...
Coptis chinensis saturated butanol dry extract (4.5~7→1)
Registrant Name : Seongil Bioex Co., Ltd.
Registration Date : 2017-12-06
Registration Number : 20171206-12-K-13-01
Manufacturer Name : Seongil Bioex Co., Ltd.
Manufacturer Address : 775 Madoro, Madoro-myeon, Hwaseong-si, Gyeonggi-do
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A butanol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of butanol, including repackagers and relabelers. The FDA regulates butanol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. butanol 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 butanol manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A butanol supplier is an individual or a company that provides butanol active pharmaceutical ingredient (API) or butanol finished formulations upon request. The butanol suppliers may include butanol API manufacturers, exporters, distributors and traders.
click here to find a list of butanol 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 butanol Drug Master File in Korea (butanol KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of butanol. The MFDS reviews the butanol KDMF as part of the drug registration process and uses the information provided in the butanol KDMF to evaluate the safety and efficacy of the drug.
After submitting a butanol 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 butanol API can apply through the Korea Drug Master File (KDMF).
click here to find a list of butanol suppliers with KDMF on PharmaCompass.
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