01 1Redox Bio Co., Ltd. @ Kyungbo Pharmaceutical Co., Ltd. @ North China Pharmaceutical Co., Ltd.
01 1Redox Bio Co., Ltd.
01 1Methylolcephalexin lysine
01 1South Korea
Registrant Name : Redox Bio Co., Ltd.
Registration Date : 2021-08-17
Registration Number : 20210817-209-J-1090
Manufacturer Name : Redox Bio Co., Ltd. @ Kyungb...
Manufacturer Address : 83, Jeyakgongdan 3-gil, Hyangnam-eup, Hwaseong-si, Gyeonggi-do @ 174, Silok-ro, Asan-...
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PharmaCompass offers a list of Cephalexin Hydrochloride 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 Cephalexin Hydrochloride manufacturer or Cephalexin Hydrochloride supplier for your needs.
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A Cephalexin Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cephalexin Hydrochloride, including repackagers and relabelers. The FDA regulates Cephalexin Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cephalexin Hydrochloride 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 Cephalexin Hydrochloride supplier is an individual or a company that provides Cephalexin Hydrochloride active pharmaceutical ingredient (API) or Cephalexin Hydrochloride finished formulations upon request. The Cephalexin Hydrochloride suppliers may include Cephalexin Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Cephalexin Hydrochloride 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 Cephalexin Hydrochloride Drug Master File in Korea (Cephalexin Hydrochloride KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Cephalexin Hydrochloride. The MFDS reviews the Cephalexin Hydrochloride KDMF as part of the drug registration process and uses the information provided in the Cephalexin Hydrochloride KDMF to evaluate the safety and efficacy of the drug.
After submitting a Cephalexin Hydrochloride 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 Cephalexin Hydrochloride API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Cephalexin Hydrochloride suppliers with KDMF on PharmaCompass.
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