01 1Juzen Chemical Co., Ltd.
01 1Thiopental sodium
01 1Japan
Registration Number : 217MF10011
Registrant's Address : 1-10 Kibacho, Toyama City, Toyama Prefecture
Initial Date of Registration : 2005-05-18
Latest Date of Registration : 2007-10-24
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PharmaCompass offers a list of Thiopental Sodium 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 Thiopental Sodium manufacturer or Thiopental Sodium supplier for your needs.
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A 5-Ethyl-5-(1-methylbutyl)-2-thiobarbituric acid monosodium manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 5-Ethyl-5-(1-methylbutyl)-2-thiobarbituric acid monosodium, including repackagers and relabelers. The FDA regulates 5-Ethyl-5-(1-methylbutyl)-2-thiobarbituric acid monosodium manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 5-Ethyl-5-(1-methylbutyl)-2-thiobarbituric acid monosodium 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 5-Ethyl-5-(1-methylbutyl)-2-thiobarbituric acid monosodium supplier is an individual or a company that provides 5-Ethyl-5-(1-methylbutyl)-2-thiobarbituric acid monosodium active pharmaceutical ingredient (API) or 5-Ethyl-5-(1-methylbutyl)-2-thiobarbituric acid monosodium finished formulations upon request. The 5-Ethyl-5-(1-methylbutyl)-2-thiobarbituric acid monosodium suppliers may include 5-Ethyl-5-(1-methylbutyl)-2-thiobarbituric acid monosodium API manufacturers, exporters, distributors and traders.
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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 5-Ethyl-5-(1-methylbutyl)-2-thiobarbituric acid monosodium Drug Master File in Japan (5-Ethyl-5-(1-methylbutyl)-2-thiobarbituric acid monosodium JDMF) empowers 5-Ethyl-5-(1-methylbutyl)-2-thiobarbituric acid monosodium 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 5-Ethyl-5-(1-methylbutyl)-2-thiobarbituric acid monosodium JDMF during the approval evaluation for pharmaceutical products. At the time of 5-Ethyl-5-(1-methylbutyl)-2-thiobarbituric acid monosodium JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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We have 1 companies offering 5-Ethyl-5-(1-methylbutyl)-2-thiobarbituric acid monosodium
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