01 1Osaka Synthetic Organic Chemistry Laboratory Co., Ltd.
01 1Stand spiron citrate production dedicated
01 1Japan
Tandospirone citrate For manufacturing purposes only
Registration Number : 228MF10016
Registrant's Address : 1-1-2 Nishinomiyahama, Nishinomiya City, Hyogo Prefecture
Initial Date of Registration : 2016-01-08
Latest Date of Registration : 2016-01-08
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PharmaCompass offers a list of Ferric Citrate 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 Ferric Citrate manufacturer or Ferric Citrate supplier for your needs.
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PharmaCompass also assists you with knowing the Ferric Citrate API Price utilized in the formulation of products. Ferric Citrate API Price is not always fixed or binding as the Ferric Citrate Price is obtained through a variety of data sources. The Ferric Citrate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Zerenex manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Zerenex, including repackagers and relabelers. The FDA regulates Zerenex manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Zerenex 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 Zerenex manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Zerenex supplier is an individual or a company that provides Zerenex active pharmaceutical ingredient (API) or Zerenex finished formulations upon request. The Zerenex suppliers may include Zerenex API manufacturers, exporters, distributors and traders.
click here to find a list of Zerenex 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 Zerenex Drug Master File in Japan (Zerenex JDMF) empowers Zerenex 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 Zerenex JDMF during the approval evaluation for pharmaceutical products. At the time of Zerenex 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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