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