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PharmaCompass offers a list of Riboflavin 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 manufacturer or Riboflavin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Riboflavin manufacturer or Riboflavin supplier.
PharmaCompass also assists you with knowing the Riboflavin API Price utilized in the formulation of products. Riboflavin API Price is not always fixed or binding as the Riboflavin Price is obtained through a variety of data sources. The Riboflavin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Vitamin B2 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Vitamin B2, including repackagers and relabelers. The FDA regulates Vitamin B2 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Vitamin B2 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 Vitamin B2 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Vitamin B2 supplier is an individual or a company that provides Vitamin B2 active pharmaceutical ingredient (API) or Vitamin B2 finished formulations upon request. The Vitamin B2 suppliers may include Vitamin B2 API manufacturers, exporters, distributors and traders.
click here to find a list of Vitamin B2 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Vitamin B2 DMF (Drug Master File) is a document detailing the whole manufacturing process of Vitamin B2 active pharmaceutical ingredient (API) in detail. Different forms of Vitamin B2 DMFs exist exist since differing nations have different regulations, such as Vitamin B2 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Vitamin B2 DMF submitted to regulatory agencies in the US is known as a USDMF. Vitamin B2 USDMF includes data on Vitamin B2's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Vitamin B2 USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Vitamin B2 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 Vitamin B2 Drug Master File in Japan (Vitamin B2 JDMF) empowers Vitamin B2 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 Vitamin B2 JDMF during the approval evaluation for pharmaceutical products. At the time of Vitamin B2 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 Vitamin B2 suppliers with JDMF on PharmaCompass.
A Vitamin B2 CEP of the European Pharmacopoeia monograph is often referred to as a Vitamin B2 Certificate of Suitability (COS). The purpose of a Vitamin B2 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Vitamin B2 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Vitamin B2 to their clients by showing that a Vitamin B2 CEP has been issued for it. The manufacturer submits a Vitamin B2 CEP (COS) as part of the market authorization procedure, and it takes on the role of a Vitamin B2 CEP holder for the record. Additionally, the data presented in the Vitamin B2 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Vitamin B2 DMF.
A Vitamin B2 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Vitamin B2 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 Vitamin B2 suppliers with CEP (COS) 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 Vitamin B2 as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Vitamin B2 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 Vitamin B2 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 Vitamin B2 and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Vitamin B2 NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Vitamin B2 suppliers with NDC on PharmaCompass.
Vitamin B2 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 Vitamin B2 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 Vitamin B2 GMP manufacturer or Vitamin B2 GMP API supplier for your needs.
A Vitamin B2 CoA (Certificate of Analysis) is a formal document that attests to Vitamin B2's compliance with Vitamin B2 specifications and serves as a tool for batch-level quality control.
Vitamin B2 CoA mostly includes findings from lab analyses of a specific batch. For each Vitamin B2 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.
Vitamin B2 may be tested according to a variety of international standards, such as European Pharmacopoeia (Vitamin B2 EP), Vitamin B2 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Vitamin B2 USP).
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