01 4FUJIFILM 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 3Sodium lactate solution
10 1Sodium lactate, Wako DL50
11 1Sodium lactate, Wako DL72
12 1Sodium lactate, Wako L50
13 1Sodium lactate, Wako L72
01 12Japan
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 : 218MF10691
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
Japanese Pharmacopoeia Sodium Lactate Solution (for manufacturing 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 Sodium Lactate Solution (50%) (For manufacturing only)
Registration Number : 228MF10227
Registrant's Address : Osaka Prefecture, Osaka City, Chuo Ward, Higashi-Koraibashi 1-16
Initial Date of Registration : 2016-12-14
Latest Date of Registration : 2016-12-14
100
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.
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A DELFLEX W/ DEXTROSE 1.5% IN PLASTIC CONTAINER-4 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of DELFLEX W/ DEXTROSE 1.5% IN PLASTIC CONTAINER-4, including repackagers and relabelers. The FDA regulates DELFLEX W/ DEXTROSE 1.5% IN PLASTIC CONTAINER-4 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. DELFLEX W/ DEXTROSE 1.5% IN PLASTIC CONTAINER-4 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 DELFLEX W/ DEXTROSE 1.5% IN PLASTIC CONTAINER-4 supplier is an individual or a company that provides DELFLEX W/ DEXTROSE 1.5% IN PLASTIC CONTAINER-4 active pharmaceutical ingredient (API) or DELFLEX W/ DEXTROSE 1.5% IN PLASTIC CONTAINER-4 finished formulations upon request. The DELFLEX W/ DEXTROSE 1.5% IN PLASTIC CONTAINER-4 suppliers may include DELFLEX W/ DEXTROSE 1.5% IN PLASTIC CONTAINER-4 API manufacturers, exporters, distributors and traders.
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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 DELFLEX W/ DEXTROSE 1.5% IN PLASTIC CONTAINER-4 Drug Master File in Japan (DELFLEX W/ DEXTROSE 1.5% IN PLASTIC CONTAINER-4 JDMF) empowers DELFLEX W/ DEXTROSE 1.5% IN PLASTIC CONTAINER-4 API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
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We have 5 companies offering DELFLEX W/ DEXTROSE 1.5% IN PLASTIC CONTAINER-4
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