01 1Kohjin Life Sciences Co., Ltd.
02 1Kyowa Hakko Bio Co., Ltd.
03 2Shandong Jincheng Bio-pharmaceutical Co. , Ltd.
01 1Glutathione
02 1Glutathione (drug substance intermediate)
03 1Japanese Pharmacopoeia glutathione
04 1Oxy glutathione Kyowa
01 2China
02 2Japan
Japanese Pharmacopoeia Glutathione
Registration Number : 217MF10303
Registrant's Address : 1-1-3 Yurakucho, Chiyoda-ku, Tokyo
Initial Date of Registration : 2005-06-30
Latest Date of Registration : 2010-03-02
Registration Number : 217MF10240
Registrant's Address : 1-6-1 Otemachi, Chiyoda-ku, Tokyo
Initial Date of Registration : 2005-06-15
Latest Date of Registration : 2014-12-08
Glutathione (pharmaceutical intermediate)
Registration Number : 304MF10007
Registrant's Address : Zichuan Economic Development Zone, Zibo City, Shandong Province, China
Initial Date of Registration : 2022-01-11
Latest Date of Registration : 2022-01-11
Registration Number : 223MF10160
Registrant's Address : Zichuan Economic Development Zone, Zibo City, Shandong Province, China
Initial Date of Registration : 2011-11-14
Latest Date of Registration : 2011-11-14
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PharmaCompass offers a list of Glutathione 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 Glutathione manufacturer or Glutathione supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Glutathione manufacturer or Glutathione supplier.
PharmaCompass also assists you with knowing the Glutathione API Price utilized in the formulation of products. Glutathione API Price is not always fixed or binding as the Glutathione Price is obtained through a variety of data sources. The Glutathione Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Ledac manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ledac, including repackagers and relabelers. The FDA regulates Ledac manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ledac 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 Ledac manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ledac supplier is an individual or a company that provides Ledac active pharmaceutical ingredient (API) or Ledac finished formulations upon request. The Ledac suppliers may include Ledac API manufacturers, exporters, distributors and traders.
click here to find a list of Ledac 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 Ledac Drug Master File in Japan (Ledac JDMF) empowers Ledac 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 Ledac JDMF during the approval evaluation for pharmaceutical products. At the time of Ledac 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 Ledac suppliers with JDMF on PharmaCompass.
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