01 1Shandong Luoxin Pharmaceutical Group Hengxin Pharmaceutical Co. , Ltd.
01 1Ceftizoxime Sodium
01 1China
Registration Number : 302MF10068
Registrant's Address : West Side of Yanbin Road, Economic Development Zone, Feixian, Linyi, Shandong Provinc...
Initial Date of Registration : 2020-06-16
Latest Date of Registration : 2020-06-16
A Ceftizoxime Sodium manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ceftizoxime Sodium, including repackagers and relabelers. The FDA regulates Ceftizoxime Sodium manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ceftizoxime 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 Ceftizoxime Sodium manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ceftizoxime Sodium supplier is an individual or a company that provides Ceftizoxime Sodium active pharmaceutical ingredient (API) or Ceftizoxime Sodium finished formulations upon request. The Ceftizoxime Sodium suppliers may include Ceftizoxime Sodium API manufacturers, exporters, distributors and traders.
click here to find a list of Ceftizoxime Sodium 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 Ceftizoxime Sodium Drug Master File in Japan (Ceftizoxime Sodium JDMF) empowers Ceftizoxime Sodium 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 Ceftizoxime Sodium JDMF during the approval evaluation for pharmaceutical products. At the time of Ceftizoxime Sodium 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 Ceftizoxime Sodium suppliers with JDMF on PharmaCompass.
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