01 1Ajinomoto Co., Inc.
02 1CHANGZHOU YABANG PHARMACEUTICAL CO. , LTD.
03 1Kanto Chemical Co., Ltd.
01 1Ecabet Sodium Hydrate
02 1Sodium hydroxide
03 1Upacyclet sodium hydrate
01 1China
02 2Japan
Registration Number : 302MF10078
Registrant's Address : 1-15-1 Kyobashi, Chuo-ku, Tokyo
Initial Date of Registration : 2020-07-06
Latest Date of Registration : 2020-07-06
Registration Number : 227MF10264
Registrant's Address : Liangchang East Road 6#, Jintan, Jiangsu Province, P. R. China
Initial Date of Registration : 2015-11-12
Latest Date of Registration : 2015-11-12
Registration Number : 222MF10182
Registrant's Address : 3-2-8 Nihonbashi Honcho, Chuo-ku, Tokyo
Initial Date of Registration : 2010-06-25
Latest Date of Registration : 2010-06-25
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PharmaCompass offers a list of Sodium Hydroxide 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 Hydroxide manufacturer or Sodium Hydroxide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Sodium Hydroxide manufacturer or Sodium Hydroxide supplier.
PharmaCompass also assists you with knowing the Sodium Hydroxide API Price utilized in the formulation of products. Sodium Hydroxide API Price is not always fixed or binding as the Sodium Hydroxide Price is obtained through a variety of data sources. The Sodium Hydroxide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A 06208_SIAL manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 06208_SIAL, including repackagers and relabelers. The FDA regulates 06208_SIAL manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 06208_SIAL API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A 06208_SIAL supplier is an individual or a company that provides 06208_SIAL active pharmaceutical ingredient (API) or 06208_SIAL finished formulations upon request. The 06208_SIAL suppliers may include 06208_SIAL API manufacturers, exporters, distributors and traders.
click here to find a list of 06208_SIAL 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 06208_SIAL Drug Master File in Japan (06208_SIAL JDMF) empowers 06208_SIAL 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 06208_SIAL JDMF during the approval evaluation for pharmaceutical products. At the time of 06208_SIAL 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 06208_SIAL suppliers with JDMF on PharmaCompass.
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