01 2Tomita Pharmaceutical Co., Ltd.
02 1Zhejiang Ruibang Laboratories
01 1Calcium Gluconate
02 1Calcium gluconate
03 1Japanese Pharmacopoeia Calcium gluconate hydrate
01 1China
02 2Japan
Registration Number : 217MF10521
Registrant's Address : Tokushima Prefecture Naruto City Setocho Myojin Maruyama 85-1
Initial Date of Registration : 2005-09-07
Latest Date of Registration : 2006-07-20
Japanese Pharmacopoeia Calcium Gluconate Hydrate
Registration Number : 306MF10018
Registrant's Address : Tokushima Prefecture Naruto City Setocho Myojin Maruyama 85-1
Initial Date of Registration : 2024-01-30
Latest Date of Registration : 2024-01-30
Registration Number : 305MF10100
Registrant's Address : No. 578, Binhai Ten Road, Economic and Technological Development Zone, Wenzhou, Zheji...
Initial Date of Registration : 2023-08-22
Latest Date of Registration : 2023-08-22
A Calcium Gluconate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Calcium Gluconate, including repackagers and relabelers. The FDA regulates Calcium Gluconate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Calcium Gluconate 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 Gluconate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Calcium Gluconate supplier is an individual or a company that provides Calcium Gluconate active pharmaceutical ingredient (API) or Calcium Gluconate finished formulations upon request. The Calcium Gluconate suppliers may include Calcium Gluconate API manufacturers, exporters, distributors and traders.
click here to find a list of Calcium Gluconate 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 Gluconate Drug Master File in Japan (Calcium Gluconate JDMF) empowers Calcium Gluconate 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 Gluconate JDMF during the approval evaluation for pharmaceutical products. At the time of Calcium Gluconate 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 Gluconate suppliers with JDMF on PharmaCompass.
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