01 1Zhejiang Dongying Pharmaceutical Co., Ltd.
01 1Daewoong Bio Co., Ltd.
01 1Cell Digitized Sodium
01 1China
Registrant Name : Daewoong Bio Co., Ltd.
Registration Date : 2019-11-19
Registration Number : 20191119-21-A-351-02
Manufacturer Name : Zhejiang Dongying Pharmaceut...
Manufacturer Address : Weiwu Road, Hangzhou Bay Shangyu Economic and Technological Development Area China
21
PharmaCompass offers a list of Cefodizime Sodium 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 Cefodizime Sodium manufacturer or Cefodizime Sodium supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Cefodizime Sodium manufacturer or Cefodizime Sodium supplier.
A cefodizime manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of cefodizime, including repackagers and relabelers. The FDA regulates cefodizime manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. cefodizime API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A cefodizime supplier is an individual or a company that provides cefodizime active pharmaceutical ingredient (API) or cefodizime finished formulations upon request. The cefodizime suppliers may include cefodizime API manufacturers, exporters, distributors and traders.
click here to find a list of cefodizime 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 cefodizime Drug Master File in Korea (cefodizime KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of cefodizime. The MFDS reviews the cefodizime KDMF as part of the drug registration process and uses the information provided in the cefodizime KDMF to evaluate the safety and efficacy of the drug.
After submitting a cefodizime 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 cefodizime API can apply through the Korea Drug Master File (KDMF).
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