01 1Dominion Salt Limited
02 2Japan Household Salt Co., Ltd.
03 1Japan Salt Manufacturing Co., Ltd.
04 1Manac Corporation
05 1Naruto Salt Co., Ltd.
06 1Salinen Austria AG
07 2Tomita Pharmaceutical Co., Ltd.
01 5Japanese Pharmacopoeia sodium chloride (production only)
02 2Sodium Chloride
03 1Sodium chloride
04 1Sodium chloride "Tomita"
01 1Austria
02 2Gabon
03 5Japan
04 1Blank
Japanese Pharmacopoeia Sodium Chloride (for manufacturing only)
Registration Number : 217MF10678
Registrant's Address : 92 Minookicho, Fukuyama City, Hiroshima Prefecture
Initial Date of Registration : 2005-10-07
Latest Date of Registration : 2006-12-18
Japanese Pharmacopoeia Sodium Chloride (for manufacturing only)
Registration Number : 217MF10793
Registrant's Address : 53 Matsushima Kurosaki, Fuyacho, Naruto City, Tokushima Prefecture
Initial Date of Registration : 2005-10-20
Latest Date of Registration : 2006-12-27
Japanese Pharmacopoeia Sodium Chloride (for manufacturing only)
Registration Number : 305MF10114
Registrant's Address : Kanagawa Prefecture Kawasaki City Kawasaki Ward Yoko 3-3-3
Initial Date of Registration : 2023-10-04
Latest Date of Registration : 2023-10-04
Registration Number : 219MF10181
Registrant's Address : Steinkogelstrasse 30, A-4802 Ebensee, Austria
Initial Date of Registration : 2007-06-01
Latest Date of Registration : 2007-06-01
Japanese Pharmacopoeia Sodium Chloride (for manufacturing only)
Registration Number : 220MF10026
Registrant's Address : Tokushima Prefecture Naruto City Setocho Myojin Maruyama 85-1
Initial Date of Registration : 2008-01-23
Latest Date of Registration : 2008-01-23
Registration Number : 217MF10520
Registrant's Address : Tokushima Prefecture Naruto City Setocho Myojin Maruyama 85-1
Initial Date of Registration : 2005-09-07
Latest Date of Registration : 2006-12-28
Japanese Pharmacopoeia Sodium Chloride (for manufacturing only)
Registration Number : 217MF11266
Registrant's Address : 2471 Munekami, Tamano City, Okayama Prefecture
Initial Date of Registration : 2005-12-20
Latest Date of Registration : 2006-10-06
Japanese Pharmacopoeia Sodium Chloride (for manufacturing only)
Registration Number : 218MF10119
Registrant's Address : 2471 Munekami, Tamano City, Okayama Prefecture
Initial Date of Registration : 2006-01-30
Latest Date of Registration : 2007-12-19
Registration Number : 306MF10054
Registrant's Address : 89 Totara Street, Mount Maunganui, New Zealand
Initial Date of Registration : 2024-04-10
Latest Date of Registration : 2024-04-10
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A Sodium Chloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sodium Chloride, including repackagers and relabelers. The FDA regulates Sodium Chloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sodium Chloride 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 Sodium Chloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Sodium Chloride supplier is an individual or a company that provides Sodium Chloride active pharmaceutical ingredient (API) or Sodium Chloride finished formulations upon request. The Sodium Chloride suppliers may include Sodium Chloride API manufacturers, exporters, distributors and traders.
click here to find a list of Sodium Chloride 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 Sodium Chloride Drug Master File in Japan (Sodium Chloride JDMF) empowers Sodium Chloride 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 Sodium Chloride JDMF during the approval evaluation for pharmaceutical products. At the time of Sodium Chloride 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 Sodium Chloride suppliers with JDMF on PharmaCompass.
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