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API SUPPLIERS
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USDMF
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Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.
About the Company : Biophore, founded in 2007, has established itself as a reliable partner in the development and manufacturing of niche and complex pharmaceutical products. With 4 USFDA and EU-appro...
LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
About the Company : LGM Pharma is a global leader in sourcing hard-to-find APIs and intermediates for the pharmaceutical and biotech industries. LGM is also a full service CDMO providing formulation, ...
HRV Global Life Sciences - Market Expansion Leader in Pharmaceuticals.
About the Company : HRV Global is a leading global manufacturer, seller & exporter of a wide range of APIs, advanced intermediates, pellets, food grade chemicals, food additives & food ingredients. It...
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ABOUT THIS PAGE
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PharmaCompass offers a list of Agomelatine 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 Agomelatine manufacturer or Agomelatine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Agomelatine manufacturer or Agomelatine supplier.
PharmaCompass also assists you with knowing the Agomelatine API Price utilized in the formulation of products. Agomelatine API Price is not always fixed or binding as the Agomelatine Price is obtained through a variety of data sources. The Agomelatine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A valdoxan manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of valdoxan, including repackagers and relabelers. The FDA regulates valdoxan manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. valdoxan 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 valdoxan manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A valdoxan supplier is an individual or a company that provides valdoxan active pharmaceutical ingredient (API) or valdoxan finished formulations upon request. The valdoxan suppliers may include valdoxan API manufacturers, exporters, distributors and traders.
click here to find a list of valdoxan suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A valdoxan DMF (Drug Master File) is a document detailing the whole manufacturing process of valdoxan active pharmaceutical ingredient (API) in detail. Different forms of valdoxan DMFs exist exist since differing nations have different regulations, such as valdoxan USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A valdoxan DMF submitted to regulatory agencies in the US is known as a USDMF. valdoxan USDMF includes data on valdoxan's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The valdoxan USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of valdoxan suppliers with USDMF on PharmaCompass.
In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a valdoxan Drug Master File in Korea (valdoxan KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of valdoxan. The MFDS reviews the valdoxan KDMF as part of the drug registration process and uses the information provided in the valdoxan KDMF to evaluate the safety and efficacy of the drug.
After submitting a valdoxan KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their valdoxan API can apply through the Korea Drug Master File (KDMF).
click here to find a list of valdoxan suppliers with KDMF on PharmaCompass.
A valdoxan written confirmation (valdoxan WC) is an official document issued by a regulatory agency to a valdoxan manufacturer, verifying that the manufacturing facility of a valdoxan active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting valdoxan APIs or valdoxan finished pharmaceutical products to another nation, regulatory agencies frequently require a valdoxan WC (written confirmation) as part of the regulatory process.
click here to find a list of valdoxan 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 valdoxan as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for valdoxan 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 valdoxan 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 valdoxan and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a valdoxan NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of valdoxan suppliers with NDC on PharmaCompass.
valdoxan 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 valdoxan 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 valdoxan GMP manufacturer or valdoxan GMP API supplier for your needs.
A valdoxan CoA (Certificate of Analysis) is a formal document that attests to valdoxan's compliance with valdoxan specifications and serves as a tool for batch-level quality control.
valdoxan CoA mostly includes findings from lab analyses of a specific batch. For each valdoxan 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.
valdoxan may be tested according to a variety of international standards, such as European Pharmacopoeia (valdoxan EP), valdoxan JP (Japanese Pharmacopeia) and the US Pharmacopoeia (valdoxan USP).
