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PharmaCompass offers a list of N-Acetyl-L-Tyrosine 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 N-Acetyl-L-Tyrosine manufacturer or N-Acetyl-L-Tyrosine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred N-Acetyl-L-Tyrosine manufacturer or N-Acetyl-L-Tyrosine supplier.
PharmaCompass also assists you with knowing the N-Acetyl-L-Tyrosine API Price utilized in the formulation of products. N-Acetyl-L-Tyrosine API Price is not always fixed or binding as the N-Acetyl-L-Tyrosine Price is obtained through a variety of data sources. The N-Acetyl-L-Tyrosine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Ethyl N-Alpha-Acetyl-Tyrosinate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ethyl N-Alpha-Acetyl-Tyrosinate, including repackagers and relabelers. The FDA regulates Ethyl N-Alpha-Acetyl-Tyrosinate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ethyl N-Alpha-Acetyl-Tyrosinate 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 Ethyl N-Alpha-Acetyl-Tyrosinate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ethyl N-Alpha-Acetyl-Tyrosinate supplier is an individual or a company that provides Ethyl N-Alpha-Acetyl-Tyrosinate active pharmaceutical ingredient (API) or Ethyl N-Alpha-Acetyl-Tyrosinate finished formulations upon request. The Ethyl N-Alpha-Acetyl-Tyrosinate suppliers may include Ethyl N-Alpha-Acetyl-Tyrosinate API manufacturers, exporters, distributors and traders.
click here to find a list of Ethyl N-Alpha-Acetyl-Tyrosinate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Ethyl N-Alpha-Acetyl-Tyrosinate DMF (Drug Master File) is a document detailing the whole manufacturing process of Ethyl N-Alpha-Acetyl-Tyrosinate active pharmaceutical ingredient (API) in detail. Different forms of Ethyl N-Alpha-Acetyl-Tyrosinate DMFs exist exist since differing nations have different regulations, such as Ethyl N-Alpha-Acetyl-Tyrosinate USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Ethyl N-Alpha-Acetyl-Tyrosinate DMF submitted to regulatory agencies in the US is known as a USDMF. Ethyl N-Alpha-Acetyl-Tyrosinate USDMF includes data on Ethyl N-Alpha-Acetyl-Tyrosinate's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Ethyl N-Alpha-Acetyl-Tyrosinate USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Ethyl N-Alpha-Acetyl-Tyrosinate suppliers with USDMF on PharmaCompass.
National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing Ethyl N-Alpha-Acetyl-Tyrosinate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Ethyl N-Alpha-Acetyl-Tyrosinate API and other APIs are published in this directory by the FDA.
The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.
Pharmaceutical companies that manufacture Ethyl N-Alpha-Acetyl-Tyrosinate as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.
The NDC directory also contains data on finished compounded human drug products that contain Ethyl N-Alpha-Acetyl-Tyrosinate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Ethyl N-Alpha-Acetyl-Tyrosinate NDC to their finished compounded human drug products, they may choose to do so.
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Ethyl N-Alpha-Acetyl-Tyrosinate 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 Ethyl N-Alpha-Acetyl-Tyrosinate 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 Ethyl N-Alpha-Acetyl-Tyrosinate GMP manufacturer or Ethyl N-Alpha-Acetyl-Tyrosinate GMP API supplier for your needs.
A Ethyl N-Alpha-Acetyl-Tyrosinate CoA (Certificate of Analysis) is a formal document that attests to Ethyl N-Alpha-Acetyl-Tyrosinate's compliance with Ethyl N-Alpha-Acetyl-Tyrosinate specifications and serves as a tool for batch-level quality control.
Ethyl N-Alpha-Acetyl-Tyrosinate CoA mostly includes findings from lab analyses of a specific batch. For each Ethyl N-Alpha-Acetyl-Tyrosinate 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.
Ethyl N-Alpha-Acetyl-Tyrosinate may be tested according to a variety of international standards, such as European Pharmacopoeia (Ethyl N-Alpha-Acetyl-Tyrosinate EP), Ethyl N-Alpha-Acetyl-Tyrosinate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Ethyl N-Alpha-Acetyl-Tyrosinate USP).