01 2Macco Organiques, s. r. o.
02 1Manac Co., Ltd.
03 2Tomita Pharmaceutical Co., Ltd.
04 2Uji Pharmaceutical Co., Ltd.
01 1Japanese Pharmacopoeia Drug potassium chloride (production only)
02 1Japanese Pharmacopoeia Potassium Chloride
03 1Japanese Pharmacopoeia Potassium Chloride (for manufacturing only)
04 1Japanese Pharmacopoeia potassium chloride (production only)
05 1Potassium Chloride
06 2Potassium chloride
01 2Czech Republic
02 5Japan
Registration Number : 227MF10169
Registrant's Address : Zahradni(') 46c,792 01 Brunta(')l, Czech Republic
Initial Date of Registration : 2015-06-18
Latest Date of Registration : 2015-06-18
Registration Number : 306MF10055
Registrant's Address : Zahradni(') 46c,792 01 Brunta(')l, Czech Republic
Initial Date of Registration : 2024-04-10
Latest Date of Registration : 2024-04-10
Japanese Pharmacopoeia Potassium Chloride (for manufacturing purposes only)
Registration Number : 217MF10675
Registrant's Address : 92 Minooki-cho, Fukuyama City, Hiroshima Prefecture
Initial Date of Registration : 2005-10-07
Latest Date of Registration : 2006-09-22
Japanese Pharmacopoeia Potassium Chloride
Registration Number : 301MF10006
Registrant's Address : 85-1 Maruyama, Myojin, Setocho, Naruto City, Tokushima Prefecture
Initial Date of Registration : 2019-05-27
Latest Date of Registration : 2019-05-27
Registration Number : 217MF10517
Registrant's Address : 85-1 Maruyama, Myojin, Setocho, Naruto City, Tokushima Prefecture
Initial Date of Registration : 2005-09-07
Latest Date of Registration : 2006-10-20
Japanese Pharmacopoeia Potassium Chloride (for manufacturing purposes only)
Registration Number : 306MF10163
Registrant's Address : 7 Kamihonjo, Myojin, Setocho, Naruto City, Tokushima Prefecture
Initial Date of Registration : 2024-12-18
Latest Date of Registration : 2024-12-18
Japanese Pharmacopoeia Potassium Chloride (for manufacturing purposes only)
Registration Number : 217MF10592
Registrant's Address : 7 Kamihonjo, Myojin, Setocho, Naruto City, Tokushima Prefecture
Initial Date of Registration : 2005-09-14
Latest Date of Registration : 2006-12-27
14
PharmaCompass offers a list of Potassium 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 Potassium Chloride manufacturer or Potassium Chloride supplier for your needs.
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A PEG 3350 AND ELECTROLYTES manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of PEG 3350 AND ELECTROLYTES, including repackagers and relabelers. The FDA regulates PEG 3350 AND ELECTROLYTES manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. PEG 3350 AND ELECTROLYTES 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 PEG 3350 AND ELECTROLYTES supplier is an individual or a company that provides PEG 3350 AND ELECTROLYTES active pharmaceutical ingredient (API) or PEG 3350 AND ELECTROLYTES finished formulations upon request. The PEG 3350 AND ELECTROLYTES suppliers may include PEG 3350 AND ELECTROLYTES 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 PEG 3350 AND ELECTROLYTES Drug Master File in Japan (PEG 3350 AND ELECTROLYTES JDMF) empowers PEG 3350 AND ELECTROLYTES 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 PEG 3350 AND ELECTROLYTES JDMF during the approval evaluation for pharmaceutical products. At the time of PEG 3350 AND ELECTROLYTES 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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