01 1Kyowa Pharma Chemical Co., Ltd.
02 1Vifor (International) Inc.
01 1Japan Pharmaceutical Codex sugar-containing iron oxide (production only)
02 1Sucroferric oxyhydroxide
01 1Japan
02 1Switzerland
Registration Number : 226MF10218
Registrant's Address : Rechenstrasse 37, CH-9001 St. Gallen
Initial Date of Registration : 2014-11-17
Latest Date of Registration : 2023-09-06
Registration Number : 217MF10117
Registrant's Address : 530 Chokeiji, Takaoka City, Toyama Prefecture
Initial Date of Registration : 2005-05-24
Latest Date of Registration : 2009-04-08
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PharmaCompass offers a list of Oxoiron 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 Oxoiron manufacturer or Oxoiron supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Oxoiron manufacturer or Oxoiron supplier.
PharmaCompass also assists you with knowing the Oxoiron API Price utilized in the formulation of products. Oxoiron API Price is not always fixed or binding as the Oxoiron Price is obtained through a variety of data sources. The Oxoiron Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Iron oxide (FeO) manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Iron oxide (FeO), including repackagers and relabelers. The FDA regulates Iron oxide (FeO) manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Iron oxide (FeO) 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 Iron oxide (FeO) supplier is an individual or a company that provides Iron oxide (FeO) active pharmaceutical ingredient (API) or Iron oxide (FeO) finished formulations upon request. The Iron oxide (FeO) suppliers may include Iron oxide (FeO) API manufacturers, exporters, distributors and traders.
click here to find a list of Iron oxide (FeO) 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 Iron oxide (FeO) Drug Master File in Japan (Iron oxide (FeO) JDMF) empowers Iron oxide (FeO) 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 Iron oxide (FeO) JDMF during the approval evaluation for pharmaceutical products. At the time of Iron oxide (FeO) 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 Iron oxide (FeO) suppliers with JDMF on PharmaCompass.
We have 2 companies offering Iron oxide (FeO)
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