01 1Osaka Synthetic Organic Chemistry Laboratory Co., Ltd.
01 1Only the Japanese Pharmacopoeia ifenprodil tartrate salt production
01 1Japan
Japanese Pharmacopoeia Ifenprodil Tartrate For manufacturing only
Registration Number : 218MF10594
Registrant's Address : 1-1-2 Nishinomiyahama, Nishinomiya City, Hyogo Prefecture
Initial Date of Registration : 2006-06-22
Latest Date of Registration : 2006-06-22
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PharmaCompass offers a list of Cerocral 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 Cerocral manufacturer or Cerocral supplier for your needs.
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PharmaCompass also assists you with knowing the Cerocral API Price utilized in the formulation of products. Cerocral API Price is not always fixed or binding as the Cerocral Price is obtained through a variety of data sources. The Cerocral Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Vadilex manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Vadilex, including repackagers and relabelers. The FDA regulates Vadilex manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Vadilex API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Vadilex supplier is an individual or a company that provides Vadilex active pharmaceutical ingredient (API) or Vadilex finished formulations upon request. The Vadilex suppliers may include Vadilex API manufacturers, exporters, distributors and traders.
click here to find a list of Vadilex 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 Vadilex Drug Master File in Japan (Vadilex JDMF) empowers Vadilex 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 Vadilex JDMF during the approval evaluation for pharmaceutical products. At the time of Vadilex 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 Vadilex suppliers with JDMF on PharmaCompass.
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