01 1Tomita Pharmaceutical Co., Ltd.
01 1Japanese Pharmacopoeia Sodium Acetate Hydrate
01 1Japan
Japanese Pharmacopoeia Sodium Acetate Hydrate
Registration Number : 305MF10045
Registrant's Address : 85-1 Maruyama, Myojin, Setocho, Naruto City, Tokushima Prefecture
Initial Date of Registration : 2023-04-05
Latest Date of Registration : 2023-04-05
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PharmaCompass offers a list of Sodium Acetate 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 Sodium Acetate manufacturer or Sodium Acetate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Sodium Acetate manufacturer or Sodium Acetate supplier.
PharmaCompass also assists you with knowing the Sodium Acetate API Price utilized in the formulation of products. Sodium Acetate API Price is not always fixed or binding as the Sodium Acetate Price is obtained through a variety of data sources. The Sodium Acetate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Sodium acetate anhydrous manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sodium acetate anhydrous, including repackagers and relabelers. The FDA regulates Sodium acetate anhydrous manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sodium acetate anhydrous 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 Sodium acetate anhydrous manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Sodium acetate anhydrous supplier is an individual or a company that provides Sodium acetate anhydrous active pharmaceutical ingredient (API) or Sodium acetate anhydrous finished formulations upon request. The Sodium acetate anhydrous suppliers may include Sodium acetate anhydrous API manufacturers, exporters, distributors and traders.
click here to find a list of Sodium acetate anhydrous 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 Sodium acetate anhydrous Drug Master File in Japan (Sodium acetate anhydrous JDMF) empowers Sodium acetate anhydrous 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 Sodium acetate anhydrous JDMF during the approval evaluation for pharmaceutical products. At the time of Sodium acetate anhydrous 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 Sodium acetate anhydrous suppliers with JDMF on PharmaCompass.
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