01 1Sinopharm Zhijun (Suzhou) Pharmaceutical Co. , Ltd.
02 2ZHEJIANG YONGNING PHARMACEUTICAL CO. , LTD.
01 3Cefpirome sulfate
01 3China
Registration Number : 220MF10013
Registrant's Address : Rich Economy District, Taicang, Jiangsu, 215416, China
Initial Date of Registration : 2008-01-09
Latest Date of Registration : 2017-01-25
Registration Number : 221MF10214
Registrant's Address : 4 MEIHUAJING ROAD, HUANGYAN, TAIZHOU, ZHEJIANG, CHINA
Initial Date of Registration : 2009-09-28
Latest Date of Registration : 2009-09-28
Registration Number : 228MF10075
Registrant's Address : 4 MEIHUAJING ROAD, HUANGYAN, TAIZHOU, ZHEJIANG, CHINA
Initial Date of Registration : 2016-03-29
Latest Date of Registration : 2016-03-29
A Cefpirome Sulphate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cefpirome Sulphate, including repackagers and relabelers. The FDA regulates Cefpirome Sulphate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cefpirome Sulphate 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 Cefpirome Sulphate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cefpirome Sulphate supplier is an individual or a company that provides Cefpirome Sulphate active pharmaceutical ingredient (API) or Cefpirome Sulphate finished formulations upon request. The Cefpirome Sulphate suppliers may include Cefpirome Sulphate API manufacturers, exporters, distributors and traders.
click here to find a list of Cefpirome Sulphate 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 Cefpirome Sulphate Drug Master File in Japan (Cefpirome Sulphate JDMF) empowers Cefpirome Sulphate 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 Cefpirome Sulphate JDMF during the approval evaluation for pharmaceutical products. At the time of Cefpirome Sulphate 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 Cefpirome Sulphate suppliers with JDMF on PharmaCompass.
We have 2 companies offering Cefpirome Sulphate
Get in contact with the supplier of your choice:
LOOKING FOR A SUPPLIER?
