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PharmaCompass offers a list of Roxarsone 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 Roxarsone manufacturer or Roxarsone supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Roxarsone manufacturer or Roxarsone supplier.
PharmaCompass also assists you with knowing the Roxarsone API Price utilized in the formulation of products. Roxarsone API Price is not always fixed or binding as the Roxarsone Price is obtained through a variety of data sources. The Roxarsone Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Roxarsone manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Roxarsone, including repackagers and relabelers. The FDA regulates Roxarsone manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Roxarsone 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 Roxarsone supplier is an individual or a company that provides Roxarsone active pharmaceutical ingredient (API) or Roxarsone finished formulations upon request. The Roxarsone suppliers may include Roxarsone API manufacturers, exporters, distributors and traders.
click here to find a list of Roxarsone suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Roxarsone DMF (Drug Master File) is a document detailing the whole manufacturing process of Roxarsone active pharmaceutical ingredient (API) in detail. Different forms of Roxarsone DMFs exist exist since differing nations have different regulations, such as Roxarsone USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Roxarsone DMF submitted to regulatory agencies in the US is known as a USDMF. Roxarsone USDMF includes data on Roxarsone's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Roxarsone USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Roxarsone suppliers with USDMF on PharmaCompass.
Roxarsone 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 Roxarsone 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 Roxarsone GMP manufacturer or Roxarsone GMP API supplier for your needs.
A Roxarsone CoA (Certificate of Analysis) is a formal document that attests to Roxarsone's compliance with Roxarsone specifications and serves as a tool for batch-level quality control.
Roxarsone CoA mostly includes findings from lab analyses of a specific batch. For each Roxarsone 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.
Roxarsone may be tested according to a variety of international standards, such as European Pharmacopoeia (Roxarsone EP), Roxarsone JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Roxarsone USP).