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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PharmaCompass also assists you with knowing the Thiopental Sodium API Price utilized in the formulation of products. Thiopental Sodium API Price is not always fixed or binding as the Thiopental Sodium Price is obtained through a variety of data sources. The Thiopental Sodium Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Sodium pentothal manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sodium pentothal, including repackagers and relabelers. The FDA regulates Sodium pentothal manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sodium pentothal 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 Sodium pentothal supplier is an individual or a company that provides Sodium pentothal active pharmaceutical ingredient (API) or Sodium pentothal finished formulations upon request. The Sodium pentothal suppliers may include Sodium pentothal API manufacturers, exporters, distributors and traders.
click here to find a list of Sodium pentothal 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 pentothal Drug Master File in Japan (Sodium pentothal JDMF) empowers Sodium pentothal 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 pentothal JDMF during the approval evaluation for pharmaceutical products. At the time of Sodium pentothal 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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