01 3Amicogen (China) Biopharm Co. , Ltd.
02 1Fujian Fukang Pharmaceutical Co. , Ltd.
01 3Cefmetazole
02 1cefmetazole acid
01 4China
Registration Number : 231MF10089
Registrant's Address : No. 1688 Shixian Road, Jining City, Shandong Province
Initial Date of Registration : 2019-04-11
Latest Date of Registration : 2019-04-11
Registration Number : 305MF10064
Registrant's Address : No. 1688 Shixian Road, Jining City, Shandong Province
Initial Date of Registration : 2023-05-17
Latest Date of Registration : 2023-05-17
Registration Number : 229MF10137
Registrant's Address : No. 6, Gaogang Avenue, Jiangyin Industrial Estate, Fuqing, Fuzhou, Fujian, China
Initial Date of Registration : 2017-07-24
Latest Date of Registration : 2017-07-24
Registration Number : 227MF10099
Registrant's Address : No. 1688 Shixian Road, Jining City, Shandong Province
Initial Date of Registration : 2015-04-09
Latest Date of Registration : 2015-04-09
A Cefmetazole manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cefmetazole, including repackagers and relabelers. The FDA regulates Cefmetazole manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cefmetazole 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 Cefmetazole supplier is an individual or a company that provides Cefmetazole active pharmaceutical ingredient (API) or Cefmetazole finished formulations upon request. The Cefmetazole suppliers may include Cefmetazole API manufacturers, exporters, distributors and traders.
click here to find a list of Cefmetazole suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The Cefmetazole Drug Master File in Japan (Cefmetazole JDMF) empowers Cefmetazole API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the Cefmetazole JDMF during the approval evaluation for pharmaceutical products. At the time of Cefmetazole JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Cefmetazole suppliers with JDMF on PharmaCompass.
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