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PharmaCompass offers a list of Riboflavin Sodium Phosphate 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 Riboflavin Sodium Phosphate manufacturer or Riboflavin Sodium Phosphate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Riboflavin Sodium Phosphate manufacturer or Riboflavin Sodium Phosphate supplier.
PharmaCompass also assists you with knowing the Riboflavin Sodium Phosphate API Price utilized in the formulation of products. Riboflavin Sodium Phosphate API Price is not always fixed or binding as the Riboflavin Sodium Phosphate Price is obtained through a variety of data sources. The Riboflavin Sodium Phosphate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Riboflavin Sodium Phosphate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Riboflavin Sodium Phosphate, including repackagers and relabelers. The FDA regulates Riboflavin Sodium Phosphate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Riboflavin Sodium Phosphate 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 Riboflavin Sodium Phosphate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Riboflavin Sodium Phosphate supplier is an individual or a company that provides Riboflavin Sodium Phosphate active pharmaceutical ingredient (API) or Riboflavin Sodium Phosphate finished formulations upon request. The Riboflavin Sodium Phosphate suppliers may include Riboflavin Sodium Phosphate API manufacturers, exporters, distributors and traders.
click here to find a list of Riboflavin Sodium Phosphate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Riboflavin Sodium Phosphate DMF (Drug Master File) is a document detailing the whole manufacturing process of Riboflavin Sodium Phosphate active pharmaceutical ingredient (API) in detail. Different forms of Riboflavin Sodium Phosphate DMFs exist exist since differing nations have different regulations, such as Riboflavin Sodium Phosphate USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Riboflavin Sodium Phosphate DMF submitted to regulatory agencies in the US is known as a USDMF. Riboflavin Sodium Phosphate USDMF includes data on Riboflavin Sodium Phosphate's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Riboflavin Sodium Phosphate USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Riboflavin Sodium Phosphate suppliers with USDMF 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 Riboflavin Sodium Phosphate Drug Master File in Japan (Riboflavin Sodium Phosphate JDMF) empowers Riboflavin Sodium Phosphate 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 Riboflavin Sodium Phosphate JDMF during the approval evaluation for pharmaceutical products. At the time of Riboflavin Sodium Phosphate 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 Riboflavin Sodium Phosphate suppliers with JDMF on PharmaCompass.
A Riboflavin Sodium Phosphate CEP of the European Pharmacopoeia monograph is often referred to as a Riboflavin Sodium Phosphate Certificate of Suitability (COS). The purpose of a Riboflavin Sodium Phosphate CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Riboflavin Sodium Phosphate EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Riboflavin Sodium Phosphate to their clients by showing that a Riboflavin Sodium Phosphate CEP has been issued for it. The manufacturer submits a Riboflavin Sodium Phosphate CEP (COS) as part of the market authorization procedure, and it takes on the role of a Riboflavin Sodium Phosphate CEP holder for the record. Additionally, the data presented in the Riboflavin Sodium Phosphate CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Riboflavin Sodium Phosphate DMF.
A Riboflavin Sodium Phosphate CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Riboflavin Sodium Phosphate CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
click here to find a list of Riboflavin Sodium Phosphate suppliers with CEP (COS) on PharmaCompass.
A Riboflavin Sodium Phosphate written confirmation (Riboflavin Sodium Phosphate WC) is an official document issued by a regulatory agency to a Riboflavin Sodium Phosphate manufacturer, verifying that the manufacturing facility of a Riboflavin Sodium Phosphate active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Riboflavin Sodium Phosphate APIs or Riboflavin Sodium Phosphate finished pharmaceutical products to another nation, regulatory agencies frequently require a Riboflavin Sodium Phosphate WC (written confirmation) as part of the regulatory process.
click here to find a list of Riboflavin Sodium Phosphate suppliers with Written Confirmation (WC) 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 Riboflavin Sodium Phosphate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Riboflavin Sodium Phosphate 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 Riboflavin Sodium Phosphate 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 Riboflavin Sodium Phosphate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Riboflavin Sodium Phosphate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Riboflavin Sodium Phosphate suppliers with NDC on PharmaCompass.
Riboflavin Sodium Phosphate 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 Riboflavin Sodium Phosphate 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 Riboflavin Sodium Phosphate GMP manufacturer or Riboflavin Sodium Phosphate GMP API supplier for your needs.
A Riboflavin Sodium Phosphate CoA (Certificate of Analysis) is a formal document that attests to Riboflavin Sodium Phosphate's compliance with Riboflavin Sodium Phosphate specifications and serves as a tool for batch-level quality control.
Riboflavin Sodium Phosphate CoA mostly includes findings from lab analyses of a specific batch. For each Riboflavin Sodium Phosphate 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.
Riboflavin Sodium Phosphate may be tested according to a variety of international standards, such as European Pharmacopoeia (Riboflavin Sodium Phosphate EP), Riboflavin Sodium Phosphate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Riboflavin Sodium Phosphate USP).