01 2Macco Organiques, s. r. o.
02 1Manac Co., Ltd.
03 1Tomita Pharmaceutical Co., Ltd.
01 1Japanese Pharmacopoeia Non-Pharmaceutical Standard Magnesium Chloride
02 1Magnesium Chloride
03 1Magnesium chloride
04 1Outsiders regulations magnesium chloride (production only)
01 2Czech Republic
02 2Japan
Registration Number : 223MF10150
Registrant's Address : Zahradni(') 46c,792 01 Brunta(')l, Czech Republic
Initial Date of Registration : 2011-10-14
Latest Date of Registration : 2020-08-27
Registration Number : 305MF10009
Registrant's Address : Zahradni(') 46c,792 01 Brunta(')l, Czech Republic
Initial Date of Registration : 2023-01-18
Latest Date of Registration : 2023-01-18
Magnesium chloride (for manufacturing purposes only)
Registration Number : 217MF10674
Registrant's Address : 92 Minooki-cho, Fukuyama City, Hiroshima Prefecture
Initial Date of Registration : 2005-10-07
Latest Date of Registration : 2006-12-28
Japanese Pharmacopoeia Non-Drug Standards Magnesium Chloride
Registration Number : 230MF10112
Registrant's Address : 85-1 Maruyama, Myojin, Setocho, Naruto City, Tokushima Prefecture
Initial Date of Registration : 2018-08-20
Latest Date of Registration : 2018-08-20
11
PharmaCompass offers a list of Magnesium 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 Magnesium Chloride manufacturer or Magnesium Chloride supplier for your needs.
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PharmaCompass also assists you with knowing the Magnesium Chloride API Price utilized in the formulation of products. Magnesium Chloride API Price is not always fixed or binding as the Magnesium Chloride Price is obtained through a variety of data sources. The Magnesium Chloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A AMINOSYN II 10% W/ ELECTROLYTES manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of AMINOSYN II 10% W/ ELECTROLYTES, including repackagers and relabelers. The FDA regulates AMINOSYN II 10% W/ ELECTROLYTES manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. AMINOSYN II 10% W/ 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 AMINOSYN II 10% W/ ELECTROLYTES supplier is an individual or a company that provides AMINOSYN II 10% W/ ELECTROLYTES active pharmaceutical ingredient (API) or AMINOSYN II 10% W/ ELECTROLYTES finished formulations upon request. The AMINOSYN II 10% W/ ELECTROLYTES suppliers may include AMINOSYN II 10% W/ 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 AMINOSYN II 10% W/ ELECTROLYTES Drug Master File in Japan (AMINOSYN II 10% W/ ELECTROLYTES JDMF) empowers AMINOSYN II 10% W/ 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 AMINOSYN II 10% W/ ELECTROLYTES JDMF during the approval evaluation for pharmaceutical products. At the time of AMINOSYN II 10% W/ 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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