01 1Kyungbo Pharmaceutical Co., Ltd@[Starting material: Sepuroxime manufacturing plant] Sinopharm Weiqida Pharmaceutical Co., Ltd
01 1Kyungbo Pharmaceutical Co., Ltd.
01 1Sepuroxime sodium
01 1South Korea
Registrant Name : Kyungbo Pharmaceutical Co., Ltd.
Registration Date : 2019-01-02
Registration Number : 20190102-210-J-292
Manufacturer Name : Kyungbo Pharmaceutical Co., ...
Manufacturer Address : 174 Silok-ro, Asan-si, Chungcheongnam-do @ [Starting material Sepuroxime manufacturin...
A Cefuroxime Sodium manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cefuroxime Sodium, including repackagers and relabelers. The FDA regulates Cefuroxime Sodium manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cefuroxime Sodium 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 Cefuroxime Sodium manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cefuroxime Sodium supplier is an individual or a company that provides Cefuroxime Sodium active pharmaceutical ingredient (API) or Cefuroxime Sodium finished formulations upon request. The Cefuroxime Sodium suppliers may include Cefuroxime Sodium API manufacturers, exporters, distributors and traders.
click here to find a list of Cefuroxime Sodium 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 Cefuroxime Sodium Drug Master File in Korea (Cefuroxime Sodium KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Cefuroxime Sodium. The MFDS reviews the Cefuroxime Sodium KDMF as part of the drug registration process and uses the information provided in the Cefuroxime Sodium KDMF to evaluate the safety and efficacy of the drug.
After submitting a Cefuroxime Sodium 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 Cefuroxime Sodium API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Cefuroxime Sodium suppliers with KDMF on PharmaCompass.
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