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01 3Macco Organiques, SRO
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01 1Daeshin Pharmaceutical Co., Ltd.
02 1Masung LS Co., Ltd.
03 1Space Industry Co., Ltd.
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01 3Magnesium chloride hexahydrate
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01 3Canada
Magnesium chloride hexahydrate
Registrant Name : Daeshin Pharmaceutical Co., Ltd.
Registration Date : 2024-04-05
Registration Number : 20230315-211-J-1461(1)
Manufacturer Name : Macco Organiques, SRO
Manufacturer Address : Zahradni 46C, 792 01, Bruntal, Czech Republic
Magnesium chloride hexahydrate
Registrant Name : Masung LS Co., Ltd.
Registration Date : 2023-03-15
Registration Number : 20230315-211-J-1461
Manufacturer Name : Macco Organiques, SRO
Manufacturer Address : Zahradni 46c, 792 01, Bruntal Czech Republic
Magnesium chloride hexahydrate
Registrant Name : Space Industry Co., Ltd.
Registration Date : 2024-07-25
Registration Number : 20230315-211-J-1461(2)
Manufacturer Name : Macco Organiques, SRO
Manufacturer Address : Zahradni 46C, 792 01, Bruntal, Czech Republic
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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.
click here to find a list of AMINOSYN II 10% W/ ELECTROLYTES manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
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.
click here to find a list of AMINOSYN II 10% W/ ELECTROLYTES suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a AMINOSYN II 10% W/ ELECTROLYTES Drug Master File in Korea (AMINOSYN II 10% W/ ELECTROLYTES KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of AMINOSYN II 10% W/ ELECTROLYTES. The MFDS reviews the AMINOSYN II 10% W/ ELECTROLYTES KDMF as part of the drug registration process and uses the information provided in the AMINOSYN II 10% W/ ELECTROLYTES KDMF to evaluate the safety and efficacy of the drug.
After submitting a AMINOSYN II 10% W/ ELECTROLYTES KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their AMINOSYN II 10% W/ ELECTROLYTES API can apply through the Korea Drug Master File (KDMF).
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