01 5Fujifilm Wako Chemical Co., Ltd.
02 3Musashino Chemical Laboratory Co., Ltd.
03 4PURAC Biochem B. V.
04 4Showa Kako Co., Ltd.
05 1Taihei Chemical Industry Co., Ltd.
01 1Japanese Pharmacopoeia L- sodium lactate solution (50%) (manufactured only)
02 1Japanese Pharmacopoeia L- sodium lactate solution (production only)
03 1L- sodium lactate solution
04 2Outsider Tadashi sodium lactate solution (produced only)
05 1PURASAL S / PF 60 (5.3)
06 1PURASAL S / PF 60 (7.4)
07 1PURASAL S PF 50
08 1PURASAL S PF 60
09 1Sodium Lactate Wako L50
10 3Sodium lactate solution
11 1Sodium lactate, Wako DL50
12 1Sodium lactate, Wako DL72
13 1Sodium lactate, Wako L50
14 1Sodium lactate, Wako L72
01 13Japan
02 4Netherlands
Registration Number : 219MF10186
Registrant's Address : P. O. BOX21, Gorinchem, The Netherlands
Initial Date of Registration : 2007-06-01
Latest Date of Registration : 2024-02-29
Registration Number : 219MF10185
Registrant's Address : P. O. BOX21, Gorinchem, The Netherlands
Initial Date of Registration : 2007-06-01
Latest Date of Registration : 2024-02-29
Registration Number : 218MF10464
Registrant's Address : P. O. BOX21, Gorinchem, The Netherlands
Initial Date of Registration : 2006-04-27
Latest Date of Registration : 2024-02-29
Registration Number : 222MF10244
Registrant's Address : P. O. BOX21, Gorinchem, The Netherlands
Initial Date of Registration : 2010-10-21
Latest Date of Registration : 2023-11-08
Registration Number : 218MF10693
Registrant's Address : 3558 Kihara, Kiyotake-cho, Miyazaki City, Miyazaki Prefecture
Initial Date of Registration : 2006-08-11
Latest Date of Registration : 2006-08-11
Registration Number : 218MF10692
Registrant's Address : 3558 Kihara, Kiyotake-cho, Miyazaki City, Miyazaki Prefecture
Initial Date of Registration : 2006-08-11
Latest Date of Registration : 2006-08-11
Registration Number : 307MF10055
Registrant's Address : 3558 Kihara, Kiyotake-cho, Miyazaki City, Miyazaki Prefecture
Initial Date of Registration : 2025-04-16
Latest Date of Registration : 2025-04-16
Japanese Pharmacopoeia Sodium L-Lactate Solution (For manufacturing purposes only)
Registration Number : 224MF10179
Registrant's Address : 1-8-2 Marunouchi, Chiyoda-ku, Tokyo
Initial Date of Registration : 2012-08-17
Latest Date of Registration : 2012-08-17
Registration Number : 223MF10062
Registrant's Address : 18-23 Yoshinocho, Suita City, Osaka Prefecture
Initial Date of Registration : 2011-05-12
Latest Date of Registration : 2023-11-08
Japanese Pharmacopoeia L-Sodium Lactate Solution (50%) (For manufacturing purposes only)
Registration Number : 228MF10227
Registrant's Address : 1-16 Higashi-Korabashi, Chuo-ku, Osaka City, Osaka Prefecture
Initial Date of Registration : 2016-12-14
Latest Date of Registration : 2016-12-14
99
PharmaCompass offers a list of Sodium Lactate 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 Lactate manufacturer or Sodium Lactate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Sodium Lactate manufacturer or Sodium Lactate supplier.
PharmaCompass also assists you with knowing the Sodium Lactate API Price utilized in the formulation of products. Sodium Lactate API Price is not always fixed or binding as the Sodium Lactate Price is obtained through a variety of data sources. The Sodium Lactate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A E325 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of E325, including repackagers and relabelers. The FDA regulates E325 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. E325 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 E325 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A E325 supplier is an individual or a company that provides E325 active pharmaceutical ingredient (API) or E325 finished formulations upon request. The E325 suppliers may include E325 API manufacturers, exporters, distributors and traders.
click here to find a list of E325 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 E325 Drug Master File in Japan (E325 JDMF) empowers E325 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 E325 JDMF during the approval evaluation for pharmaceutical products. At the time of E325 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 E325 suppliers with JDMF on PharmaCompass.
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