API Suppliers
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PharmaCompass offers a list of Menadione 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 Menadione manufacturer or Menadione supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Menadione manufacturer or Menadione supplier.
PharmaCompass also assists you with knowing the Menadione API Price utilized in the formulation of products. Menadione API Price is not always fixed or binding as the Menadione Price is obtained through a variety of data sources. The Menadione Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Menadione manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Menadione, including repackagers and relabelers. The FDA regulates Menadione manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Menadione 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 Menadione manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Menadione supplier is an individual or a company that provides Menadione active pharmaceutical ingredient (API) or Menadione finished formulations upon request. The Menadione suppliers may include Menadione API manufacturers, exporters, distributors and traders.
click here to find a list of Menadione suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
Menadione 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 Menadione 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 Menadione GMP manufacturer or Menadione GMP API supplier for your needs.
A Menadione CoA (Certificate of Analysis) is a formal document that attests to Menadione's compliance with Menadione specifications and serves as a tool for batch-level quality control.
Menadione CoA mostly includes findings from lab analyses of a specific batch. For each Menadione 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.
Menadione may be tested according to a variety of international standards, such as European Pharmacopoeia (Menadione EP), Menadione JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Menadione USP).