01 1Ako Kasei Co., Ltd.
02 1Macco Organiques, s. r. o.
03 1Tomita Pharmaceutical Co., Ltd.
01 1Calcium chloride hydrate
02 1Calcium chloride, "Tomita"
03 1Japanese Pharmacopoeia calcium chloride hydrate
01 1Czech Republic
02 2Japan
Japanese Pharmacopoeia Calcium Chloride Hydrate
Registration Number : 229MF10097
Registrant's Address : 329 Sakakoshi, Ako City, Hyogo Prefecture
Initial Date of Registration : 2017-05-16
Latest Date of Registration : 2017-05-16
Registration Number : 223MF10151
Registrant's Address : Zahradni(') 46c,792 01 Brunta(')l, Czech Republic
Initial Date of Registration : 2011-10-14
Latest Date of Registration : 2020-12-18
Registration Number : 217MF10519
Registrant's Address : Tokushima Prefecture Naruto City Setocho Myojin Maruyama 85-1
Initial Date of Registration : 2005-09-07
Latest Date of Registration : 2006-12-27
A Calcium Chloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Calcium Chloride, including repackagers and relabelers. The FDA regulates Calcium Chloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Calcium Chloride 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 Calcium Chloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Calcium Chloride supplier is an individual or a company that provides Calcium Chloride active pharmaceutical ingredient (API) or Calcium Chloride finished formulations upon request. The Calcium Chloride suppliers may include Calcium Chloride API manufacturers, exporters, distributors and traders.
click here to find a list of Calcium Chloride 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 Calcium Chloride Drug Master File in Japan (Calcium Chloride JDMF) empowers Calcium Chloride 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 Calcium Chloride JDMF during the approval evaluation for pharmaceutical products. At the time of Calcium Chloride 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 Calcium Chloride suppliers with JDMF on PharmaCompass.
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