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