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API SUPPLIERS
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients, & custom-made solutions to our customers.
CEP/COS 
JDMF
NDC
ASMF
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USDMF
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Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients, & custom-made solutions to our customers.
Certificate Number : R1-CEP 2015-165 - Rev 00
Status : Valid
Issue Date : 2021-06-08
Type : Chemical
Substance Number : 2650
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Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients, & custom-made solutions to our customers.
Registration Number : 218MF10151
Registrant's Address : 23, rue Bossuet Z. I. de la Vigne aux Loups F-91160 LONGJUMEAU France
Initial Date of Registration : 2006-01-31
Latest Date of Registration : 2010-02-23
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PharmaCompass offers a list of Alimemazine 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 Alimemazine manufacturer or Alimemazine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Alimemazine manufacturer or Alimemazine supplier.
PharmaCompass also assists you with knowing the Alimemazine API Price utilized in the formulation of products. Alimemazine API Price is not always fixed or binding as the Alimemazine Price is obtained through a variety of data sources. The Alimemazine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Trimeprazine Tartrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Trimeprazine Tartrate, including repackagers and relabelers. The FDA regulates Trimeprazine Tartrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Trimeprazine Tartrate 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 Trimeprazine Tartrate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Trimeprazine Tartrate supplier is an individual or a company that provides Trimeprazine Tartrate active pharmaceutical ingredient (API) or Trimeprazine Tartrate finished formulations upon request. The Trimeprazine Tartrate suppliers may include Trimeprazine Tartrate API manufacturers, exporters, distributors and traders.
click here to find a list of Trimeprazine Tartrate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Trimeprazine Tartrate DMF (Drug Master File) is a document detailing the whole manufacturing process of Trimeprazine Tartrate active pharmaceutical ingredient (API) in detail. Different forms of Trimeprazine Tartrate DMFs exist exist since differing nations have different regulations, such as Trimeprazine Tartrate USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Trimeprazine Tartrate DMF submitted to regulatory agencies in the US is known as a USDMF. Trimeprazine Tartrate USDMF includes data on Trimeprazine Tartrate's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Trimeprazine Tartrate USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Trimeprazine Tartrate suppliers with USDMF on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The Trimeprazine Tartrate Drug Master File in Japan (Trimeprazine Tartrate JDMF) empowers Trimeprazine Tartrate API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the Trimeprazine Tartrate JDMF during the approval evaluation for pharmaceutical products. At the time of Trimeprazine Tartrate JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Trimeprazine Tartrate suppliers with JDMF on PharmaCompass.
A Trimeprazine Tartrate CEP of the European Pharmacopoeia monograph is often referred to as a Trimeprazine Tartrate Certificate of Suitability (COS). The purpose of a Trimeprazine Tartrate CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Trimeprazine Tartrate EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Trimeprazine Tartrate to their clients by showing that a Trimeprazine Tartrate CEP has been issued for it. The manufacturer submits a Trimeprazine Tartrate CEP (COS) as part of the market authorization procedure, and it takes on the role of a Trimeprazine Tartrate CEP holder for the record. Additionally, the data presented in the Trimeprazine Tartrate CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Trimeprazine Tartrate DMF.
A Trimeprazine Tartrate CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Trimeprazine Tartrate CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
click here to find a list of Trimeprazine Tartrate suppliers with CEP (COS) on PharmaCompass.
A Trimeprazine Tartrate written confirmation (Trimeprazine Tartrate WC) is an official document issued by a regulatory agency to a Trimeprazine Tartrate manufacturer, verifying that the manufacturing facility of a Trimeprazine Tartrate active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Trimeprazine Tartrate APIs or Trimeprazine Tartrate finished pharmaceutical products to another nation, regulatory agencies frequently require a Trimeprazine Tartrate WC (written confirmation) as part of the regulatory process.
click here to find a list of Trimeprazine Tartrate suppliers with Written Confirmation (WC) 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 Trimeprazine Tartrate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Trimeprazine Tartrate 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 Trimeprazine Tartrate 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 Trimeprazine Tartrate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Trimeprazine Tartrate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Trimeprazine Tartrate suppliers with NDC on PharmaCompass.
Trimeprazine Tartrate 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 Trimeprazine Tartrate 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 Trimeprazine Tartrate GMP manufacturer or Trimeprazine Tartrate GMP API supplier for your needs.
A Trimeprazine Tartrate CoA (Certificate of Analysis) is a formal document that attests to Trimeprazine Tartrate's compliance with Trimeprazine Tartrate specifications and serves as a tool for batch-level quality control.
Trimeprazine Tartrate CoA mostly includes findings from lab analyses of a specific batch. For each Trimeprazine Tartrate 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.
Trimeprazine Tartrate may be tested according to a variety of international standards, such as European Pharmacopoeia (Trimeprazine Tartrate EP), Trimeprazine Tartrate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Trimeprazine Tartrate USP).
