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