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PharmaCompass offers a list of Vildagliptin 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 Vildagliptin manufacturer or Vildagliptin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Vildagliptin manufacturer or Vildagliptin supplier.
PharmaCompass also assists you with knowing the Vildagliptin API Price utilized in the formulation of products. Vildagliptin API Price is not always fixed or binding as the Vildagliptin Price is obtained through a variety of data sources. The Vildagliptin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Xiliarx manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Xiliarx, including repackagers and relabelers. The FDA regulates Xiliarx manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Xiliarx 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 Xiliarx manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Xiliarx supplier is an individual or a company that provides Xiliarx active pharmaceutical ingredient (API) or Xiliarx finished formulations upon request. The Xiliarx suppliers may include Xiliarx API manufacturers, exporters, distributors and traders.
click here to find a list of Xiliarx suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Xiliarx DMF (Drug Master File) is a document detailing the whole manufacturing process of Xiliarx active pharmaceutical ingredient (API) in detail. Different forms of Xiliarx DMFs exist exist since differing nations have different regulations, such as Xiliarx USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Xiliarx DMF submitted to regulatory agencies in the US is known as a USDMF. Xiliarx USDMF includes data on Xiliarx's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Xiliarx USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Xiliarx 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 Xiliarx Drug Master File in Japan (Xiliarx JDMF) empowers Xiliarx 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 Xiliarx JDMF during the approval evaluation for pharmaceutical products. At the time of Xiliarx 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 Xiliarx suppliers with JDMF 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 Xiliarx Drug Master File in Korea (Xiliarx KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Xiliarx. The MFDS reviews the Xiliarx KDMF as part of the drug registration process and uses the information provided in the Xiliarx KDMF to evaluate the safety and efficacy of the drug.
After submitting a Xiliarx 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 Xiliarx API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Xiliarx suppliers with KDMF on PharmaCompass.
A Xiliarx written confirmation (Xiliarx WC) is an official document issued by a regulatory agency to a Xiliarx manufacturer, verifying that the manufacturing facility of a Xiliarx active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Xiliarx APIs or Xiliarx finished pharmaceutical products to another nation, regulatory agencies frequently require a Xiliarx WC (written confirmation) as part of the regulatory process.
click here to find a list of Xiliarx 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 Xiliarx as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Xiliarx 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 Xiliarx 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 Xiliarx and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Xiliarx NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Xiliarx suppliers with NDC on PharmaCompass.
Xiliarx 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 Xiliarx 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 Xiliarx GMP manufacturer or Xiliarx GMP API supplier for your needs.
A Xiliarx CoA (Certificate of Analysis) is a formal document that attests to Xiliarx's compliance with Xiliarx specifications and serves as a tool for batch-level quality control.
Xiliarx CoA mostly includes findings from lab analyses of a specific batch. For each Xiliarx 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.
Xiliarx may be tested according to a variety of international standards, such as European Pharmacopoeia (Xiliarx EP), Xiliarx JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Xiliarx USP).
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