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PharmaCompass offers a list of Phenethylamine 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 Phenethylamine manufacturer or Phenethylamine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Phenethylamine manufacturer or Phenethylamine supplier.
PharmaCompass also assists you with knowing the Phenethylamine API Price utilized in the formulation of products. Phenethylamine API Price is not always fixed or binding as the Phenethylamine Price is obtained through a variety of data sources. The Phenethylamine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A 1-Phenyl-2-aminoethane hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 1-Phenyl-2-aminoethane hydrochloride, including repackagers and relabelers. The FDA regulates 1-Phenyl-2-aminoethane hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 1-Phenyl-2-aminoethane hydrochloride 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-aminoethane hydrochloride supplier is an individual or a company that provides 1-Phenyl-2-aminoethane hydrochloride active pharmaceutical ingredient (API) or 1-Phenyl-2-aminoethane hydrochloride finished formulations upon request. The 1-Phenyl-2-aminoethane hydrochloride suppliers may include 1-Phenyl-2-aminoethane hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of 1-Phenyl-2-aminoethane hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A 1-Phenyl-2-aminoethane hydrochloride DMF (Drug Master File) is a document detailing the whole manufacturing process of 1-Phenyl-2-aminoethane hydrochloride active pharmaceutical ingredient (API) in detail. Different forms of 1-Phenyl-2-aminoethane hydrochloride DMFs exist exist since differing nations have different regulations, such as 1-Phenyl-2-aminoethane hydrochloride USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A 1-Phenyl-2-aminoethane hydrochloride DMF submitted to regulatory agencies in the US is known as a USDMF. 1-Phenyl-2-aminoethane hydrochloride USDMF includes data on 1-Phenyl-2-aminoethane hydrochloride's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The 1-Phenyl-2-aminoethane hydrochloride USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of 1-Phenyl-2-aminoethane hydrochloride suppliers with USDMF on PharmaCompass.
1-Phenyl-2-aminoethane hydrochloride 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-aminoethane hydrochloride 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-aminoethane hydrochloride GMP manufacturer or 1-Phenyl-2-aminoethane hydrochloride GMP API supplier for your needs.
A 1-Phenyl-2-aminoethane hydrochloride CoA (Certificate of Analysis) is a formal document that attests to 1-Phenyl-2-aminoethane hydrochloride's compliance with 1-Phenyl-2-aminoethane hydrochloride specifications and serves as a tool for batch-level quality control.
1-Phenyl-2-aminoethane hydrochloride CoA mostly includes findings from lab analyses of a specific batch. For each 1-Phenyl-2-aminoethane hydrochloride 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-aminoethane hydrochloride may be tested according to a variety of international standards, such as European Pharmacopoeia (1-Phenyl-2-aminoethane hydrochloride EP), 1-Phenyl-2-aminoethane hydrochloride JP (Japanese Pharmacopeia) and the US Pharmacopoeia (1-Phenyl-2-aminoethane hydrochloride USP).
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