01 1ACS DOBFAR SPA
02 1International Pharmaceutical Co., Ltd.
03 1SPC Co., Ltd.
01 1International Pharmaceutical Co., Ltd.
02 1SPC Co., Ltd.
03 1Sungjin Exim Co., Ltd.
01 3Cellotetan
01 1Italy
02 2South Korea
Registrant Name : Sungjin Exim Co., Ltd.
Registration Date : 2022-06-15
Registration Number : 20220615-210-J-1316
Manufacturer Name : ACS DOBFAR SPA
Manufacturer Address : Via Marzabotto 1,7/9 – 20871 Vimercate (MB), Italy
Registrant Name : International Pharmaceutical Co., Ltd.
Registration Date : 2019-12-05
Registration Number : 20191205-210-J-491
Manufacturer Name : International Pharmaceutical...
Manufacturer Address : 47 Sanseong-ro, Danwon-gu, Ansan-si, Gyeonggi-do
Registrant Name : SPC Co., Ltd.
Registration Date : 2022-11-17
Registration Number : 20221117-210-J-1405
Manufacturer Name : SPC Co., Ltd.
Manufacturer Address : 386 Pyeongtaek Port Road, Poseung-eup, Pyeongtaek-si, Gyeonggi-do
A Cefotetan manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cefotetan, including repackagers and relabelers. The FDA regulates Cefotetan manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cefotetan 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 Cefotetan manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cefotetan supplier is an individual or a company that provides Cefotetan active pharmaceutical ingredient (API) or Cefotetan finished formulations upon request. The Cefotetan suppliers may include Cefotetan API manufacturers, exporters, distributors and traders.
click here to find a list of Cefotetan 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 Cefotetan Drug Master File in Korea (Cefotetan KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Cefotetan. The MFDS reviews the Cefotetan KDMF as part of the drug registration process and uses the information provided in the Cefotetan KDMF to evaluate the safety and efficacy of the drug.
After submitting a Cefotetan 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 Cefotetan API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Cefotetan suppliers with KDMF on PharmaCompass.
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