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
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 : 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
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
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PharmaCompass offers a list of Calcium Gluconate 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 Calcium Gluconate manufacturer or Calcium Gluconate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Calcium Gluconate manufacturer or Calcium Gluconate supplier.
PharmaCompass also assists you with knowing the Calcium Gluconate API Price utilized in the formulation of products. Calcium Gluconate API Price is not always fixed or binding as the Calcium Gluconate Price is obtained through a variety of data sources. The Calcium Gluconate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Flopak Plain manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Flopak Plain, including repackagers and relabelers. The FDA regulates Flopak Plain manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Flopak Plain 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 Flopak Plain manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Flopak Plain supplier is an individual or a company that provides Flopak Plain active pharmaceutical ingredient (API) or Flopak Plain finished formulations upon request. The Flopak Plain suppliers may include Flopak Plain API manufacturers, exporters, distributors and traders.
click here to find a list of Flopak Plain 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 Flopak Plain Drug Master File in Japan (Flopak Plain JDMF) empowers Flopak Plain 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 Flopak Plain JDMF during the approval evaluation for pharmaceutical products. At the time of Flopak Plain 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 Flopak Plain suppliers with JDMF on PharmaCompass.
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