01 1Dominion Salt Limited
02 1Japan Salt Manufacturing Co., Ltd.
03 1Manac Co., Ltd.
04 1Naruto Salt Co., Ltd.
05 1Salinen Austria AG
06 2Tomita Pharmaceutical Co., Ltd.
01 3Japanese Pharmacopoeia sodium chloride (production only)
02 2Sodium Chloride
03 1Sodium chloride
04 1Sodium chloride "Tomita"
01 1Austria
02 5Japan
03 1Blank
Japanese Pharmacopoeia Sodium Chloride (for manufacturing purposes only)
Registration Number : 217MF10678
Registrant's Address : 92 Minooki-cho, Fukuyama City, Hiroshima Prefecture
Initial Date of Registration : 2005-10-07
Latest Date of Registration : 2006-12-18
Japanese Pharmacopoeia Sodium Chloride (for manufacturing purposes only)
Registration Number : 217MF10793
Registrant's Address : 53 Matsushima, Kurosaki, Muyacho, Naruto City, Tokushima Prefecture
Initial Date of Registration : 2005-10-20
Latest Date of Registration : 2006-12-27
Japanese Pharmacopoeia Sodium Chloride (for manufacturing purposes only)
Registration Number : 305MF10114
Registrant's Address : 3-3-3 Yoko, Kawasaki-ku, Kawasaki City, Kanagawa Prefecture
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 purposes only)
Registration Number : 220MF10026
Registrant's Address : 85-1 Maruyama, Myojin, Setocho, Naruto City, Tokushima Prefecture
Initial Date of Registration : 2008-01-23
Latest Date of Registration : 2008-01-23
Registration Number : 217MF10520
Registrant's Address : 85-1 Maruyama, Myojin, Setocho, Naruto City, Tokushima Prefecture
Initial Date of Registration : 2005-09-07
Latest Date of Registration : 2006-12-28
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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PharmaCompass offers a list of Sodium Chloride 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 Sodium Chloride manufacturer or Sodium Chloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Sodium Chloride manufacturer or Sodium Chloride supplier.
PharmaCompass also assists you with knowing the Sodium Chloride API Price utilized in the formulation of products. Sodium Chloride API Price is not always fixed or binding as the Sodium Chloride Price is obtained through a variety of data sources. The Sodium Chloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Purex manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Purex, including repackagers and relabelers. The FDA regulates Purex manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Purex 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 Purex manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Purex supplier is an individual or a company that provides Purex active pharmaceutical ingredient (API) or Purex finished formulations upon request. The Purex suppliers may include Purex API manufacturers, exporters, distributors and traders.
click here to find a list of Purex 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 Purex Drug Master File in Japan (Purex JDMF) empowers Purex 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 Purex JDMF during the approval evaluation for pharmaceutical products. At the time of Purex JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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