01 1ACS DOBFAR S. p. A.
02 1CSPC Zhongnuo Pharmaceutical (Shijiazhuang) Co. , Ltd.
03 2Harbin Hejia Pharmaceutical Co. , Ltd.
04 1Naturex Inc.
05 1Olon S. p. A.
06 1Orchid Pharma Limited
07 1Shenyang Sanjiu Pharmaceutical Co. , Ltd.
01 2Cefazolin Sodium
02 3Cefazolin sodium
03 1Cefazolin sodium (manufacturing only)
04 1Japanese Pharmacopoeia Cefazolin Sodium
05 1Outsiders regulations Kasansuranoru (production only)
01 4China
02 1France
03 1India
04 2Italy
Registration Number : 222MF10020
Registrant's Address : Viale Addetta, 4/12, 20067 Tribiano (Milan) Italy
Initial Date of Registration : 2010-01-22
Latest Date of Registration : 2016-08-08
Cefazolin Sodium (for manufacturing only)
Registration Number : 301MF10089
Registrant's Address : No. 88 Yangzi Road, Economic & Technological Development Zone, Shijiazhuang City, Heb...
Initial Date of Registration : 2019-11-11
Latest Date of Registration : 2021-06-07
Japanese Pharmacopoeia Cefazolin Sodium
Registration Number : 303MF10158
Registrant's Address : Economic and Technological Development Zone Shangzhi city, Heilongjiang
Initial Date of Registration : 2021-10-13
Latest Date of Registration : 2021-10-13
Registration Number : 303MF10145
Registrant's Address : Economic and Technological Development Zone Shangzhi city, Heilongjiang
Initial Date of Registration : 2021-09-09
Latest Date of Registration : 2021-09-09
Extra-official regulations Casanthranol (for manufacturing only)
Registration Number : 222MF10124
Registrant's Address : 375 Huyler Street, South Hackensack, NJ 07606, USA
Initial Date of Registration : 2010-04-05
Latest Date of Registration : 2010-04-05
Registration Number : 219MF10323
Registrant's Address : Strada Rivoltana Km 6/7 20053 Rodano Milano Italy
Initial Date of Registration : 2007-10-24
Latest Date of Registration : 2020-09-24
Registration Number : 219MF10345
Registrant's Address : 'Orchid Towers', 313, Valuvar Kottam High Road, Nungambakkam, Chennai-600 034, India
Initial Date of Registration : 2007-11-21
Latest Date of Registration : 2018-12-04
Registration Number : 305MF10056
Registrant's Address : No. 7, Dongying North 1st Road, Xinmin Economic Development Zone, Shenyang City, Liao...
Initial Date of Registration : 2023-05-10
Latest Date of Registration : 2023-05-10
95
PharmaCompass offers a list of Cefazolin Sodium API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Cefazolin Sodium manufacturer or Cefazolin Sodium supplier for your needs.
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A Cefazolin Sodium manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cefazolin Sodium, including repackagers and relabelers. The FDA regulates Cefazolin Sodium manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cefazolin 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.
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A Cefazolin Sodium supplier is an individual or a company that provides Cefazolin Sodium active pharmaceutical ingredient (API) or Cefazolin Sodium finished formulations upon request. The Cefazolin Sodium suppliers may include Cefazolin Sodium API manufacturers, exporters, distributors and traders.
click here to find a list of Cefazolin 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 Cefazolin Sodium Drug Master File in Japan (Cefazolin Sodium JDMF) empowers Cefazolin 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 Cefazolin Sodium JDMF during the approval evaluation for pharmaceutical products. At the time of Cefazolin 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 Cefazolin Sodium suppliers with JDMF on PharmaCompass.
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