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PharmaCompass offers a list of Norephedrane 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 Norephedrane manufacturer or Norephedrane supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Norephedrane manufacturer or Norephedrane supplier.
PharmaCompass also assists you with knowing the Norephedrane API Price utilized in the formulation of products. Norephedrane API Price is not always fixed or binding as the Norephedrane Price is obtained through a variety of data sources. The Norephedrane Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A 1-Phenyl-2-aminopropane manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 1-Phenyl-2-aminopropane, including repackagers and relabelers. The FDA regulates 1-Phenyl-2-aminopropane manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 1-Phenyl-2-aminopropane 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 1-Phenyl-2-aminopropane supplier is an individual or a company that provides 1-Phenyl-2-aminopropane active pharmaceutical ingredient (API) or 1-Phenyl-2-aminopropane finished formulations upon request. The 1-Phenyl-2-aminopropane suppliers may include 1-Phenyl-2-aminopropane API manufacturers, exporters, distributors and traders.
1-Phenyl-2-aminopropane 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 1-Phenyl-2-aminopropane 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 1-Phenyl-2-aminopropane GMP manufacturer or 1-Phenyl-2-aminopropane GMP API supplier for your needs.
A 1-Phenyl-2-aminopropane CoA (Certificate of Analysis) is a formal document that attests to 1-Phenyl-2-aminopropane's compliance with 1-Phenyl-2-aminopropane specifications and serves as a tool for batch-level quality control.
1-Phenyl-2-aminopropane CoA mostly includes findings from lab analyses of a specific batch. For each 1-Phenyl-2-aminopropane 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.
1-Phenyl-2-aminopropane may be tested according to a variety of international standards, such as European Pharmacopoeia (1-Phenyl-2-aminopropane EP), 1-Phenyl-2-aminopropane JP (Japanese Pharmacopeia) and the US Pharmacopoeia (1-Phenyl-2-aminopropane USP).