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