01 1Ercros SA
02 1Joyang Laboratories
01 1Aging Life Science Co., Ltd.
02 1Sam-O Pharmaceutical Co., Ltd.
01 1Sodium fusidate
02 1sodium fusidate
01 1China
02 1Spain
Registrant Name : Sam-O Pharmaceutical Co., Ltd.
Registration Date : 2019-04-22
Registration Number : 20190422-209-J-87
Manufacturer Name : Ercros SA
Manufacturer Address : Paseo del Deleite s/n, Aranjuez 28300 Madrid Spain
Registrant Name : Aging Life Science Co., Ltd.
Registration Date : 2024-10-31
Registration Number : 20241031-209-J-1707
Manufacturer Name : Joyang Laboratories
Manufacturer Address : No. 9 Haidu North Road, Sheyang Economic Development zone, Yancheng, Jiangsu, 224300 ...
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PharmaCompass offers a list of Sodium Fusidate 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 Sodium Fusidate manufacturer or Sodium Fusidate supplier for your needs.
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A Sodium Fusidate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sodium Fusidate, including repackagers and relabelers. The FDA regulates Sodium Fusidate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sodium Fusidate 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 Sodium Fusidate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Sodium Fusidate supplier is an individual or a company that provides Sodium Fusidate active pharmaceutical ingredient (API) or Sodium Fusidate finished formulations upon request. The Sodium Fusidate suppliers may include Sodium Fusidate API manufacturers, exporters, distributors and traders.
click here to find a list of Sodium Fusidate 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 Sodium Fusidate Drug Master File in Korea (Sodium Fusidate KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Sodium Fusidate. The MFDS reviews the Sodium Fusidate KDMF as part of the drug registration process and uses the information provided in the Sodium Fusidate KDMF to evaluate the safety and efficacy of the drug.
After submitting a Sodium Fusidate 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 Sodium Fusidate API can apply through the Korea Drug Master File (KDMF).
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