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PharmaCompass offers a list of Ferric Pyrophosphate 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 Pyrophosphate Citrate manufacturer or Ferric Pyrophosphate Citrate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Ferric Pyrophosphate Citrate manufacturer or Ferric Pyrophosphate Citrate supplier.
PharmaCompass also assists you with knowing the Ferric Pyrophosphate Citrate API Price utilized in the formulation of products. Ferric Pyrophosphate Citrate API Price is not always fixed or binding as the Ferric Pyrophosphate Citrate Price is obtained through a variety of data sources. The Ferric Pyrophosphate Citrate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Triferic manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Triferic, including repackagers and relabelers. The FDA regulates Triferic manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Triferic 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 Triferic manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Triferic supplier is an individual or a company that provides Triferic active pharmaceutical ingredient (API) or Triferic finished formulations upon request. The Triferic suppliers may include Triferic API manufacturers, exporters, distributors and traders.
click here to find a list of Triferic suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing Triferic as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Triferic API and other APIs are published in this directory by the FDA.
The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.
Pharmaceutical companies that manufacture Triferic as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.
The NDC directory also contains data on finished compounded human drug products that contain Triferic and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Triferic NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Triferic suppliers with NDC on PharmaCompass.
Triferic Active pharmaceutical ingredient (API) is produced in GMP-certified manufacturing facility.
GMP stands for Good Manufacturing Practices, which is a system used in the pharmaceutical industry to make sure that goods are regularly produced and monitored in accordance with quality standards. The FDA’s current Good Manufacturing Practices requirements are referred to as cGMP or current GMP which indicates that the company follows the most recent GMP specifications. The World Health Organization (WHO) has its own set of GMP guidelines, called the WHO GMP. Different countries can also set their own guidelines for GMP like China (Chinese GMP) or the EU (EU GMP).
PharmaCompass offers a list of Triferic GMP manufacturers, exporters & distributors, which can be sorted by USDMF, JDMF, KDMF, CEP (COS), WC, API price, and more, enabling you to easily find the right Triferic GMP manufacturer or Triferic GMP API supplier for your needs.
A Triferic CoA (Certificate of Analysis) is a formal document that attests to Triferic's compliance with Triferic specifications and serves as a tool for batch-level quality control.
Triferic CoA mostly includes findings from lab analyses of a specific batch. For each Triferic CoA document that a company creates, the USFDA specifies specific requirements, such as supplier information, material identification, transportation data, evidence of conformity and signature data.
Triferic may be tested according to a variety of international standards, such as European Pharmacopoeia (Triferic EP), Triferic JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Triferic USP).
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