01 1Assia Chemical Industries Ltd.
01 1Modafinil "Teva"
01 1Israel
Registration Number : 227MF10270
Registrant's Address : Neot-Hovav Eco-Industrial Park, Emek Sara P. O. Box 2049 Be'er Sheva 8412316, Israel
Initial Date of Registration : 2015-11-19
Latest Date of Registration : 2023-07-19
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PharmaCompass offers a list of Modafinil 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 Modafinil manufacturer or Modafinil supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Modafinil manufacturer or Modafinil supplier.
PharmaCompass also assists you with knowing the Modafinil API Price utilized in the formulation of products. Modafinil API Price is not always fixed or binding as the Modafinil Price is obtained through a variety of data sources. The Modafinil Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Stavigile manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Stavigile, including repackagers and relabelers. The FDA regulates Stavigile manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Stavigile 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 Stavigile manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Stavigile supplier is an individual or a company that provides Stavigile active pharmaceutical ingredient (API) or Stavigile finished formulations upon request. The Stavigile suppliers may include Stavigile API manufacturers, exporters, distributors and traders.
click here to find a list of Stavigile 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 Stavigile Drug Master File in Japan (Stavigile JDMF) empowers Stavigile 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 Stavigile JDMF during the approval evaluation for pharmaceutical products. At the time of Stavigile 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 Stavigile suppliers with JDMF on PharmaCompass.
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