01 1Tomita Pharmaceutical Co., Ltd.
01 1Japanese Pharmacopoeia Sodium Acetate Hydrate
01 1Japan
Japanese Pharmacopoeia Sodium Acetate Hydrate
Registration Number : 305MF10045
Registrant's Address : Tokushima Prefecture Naruto City Setocho Myojin Maruyama 85-1
Initial Date of Registration : 2023-04-05
Latest Date of Registration : 2023-04-05
A Sodium Acetate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sodium Acetate, including repackagers and relabelers. The FDA regulates Sodium Acetate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sodium Acetate 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 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Sodium Acetate supplier is an individual or a company that provides Sodium Acetate active pharmaceutical ingredient (API) or Sodium Acetate finished formulations upon request. The Sodium Acetate suppliers may include Sodium Acetate API manufacturers, exporters, distributors and traders.
click here to find a list of Sodium Acetate 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 Drug Master File in Japan (Sodium Acetate JDMF) empowers Sodium Acetate 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 JDMF during the approval evaluation for pharmaceutical products. At the time of Sodium Acetate 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 suppliers with JDMF on PharmaCompass.
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