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