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API SUPPLIERS
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USDMF
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DOSAGE - TABLET;ORAL - EQ 12.5MG BASE;1GM
USFDA APPLICATION NUMBER - 203414
DOSAGE - TABLET;ORAL - EQ 12.5MG BASE;500MG
USFDA APPLICATION NUMBER - 203414
DOSAGE - TABLET;ORAL - EQ 12.5MG BASE
USFDA APPLICATION NUMBER - 22271
DOSAGE - TABLET;ORAL - EQ 25MG BASE
USFDA APPLICATION NUMBER - 22271
DOSAGE - TABLET;ORAL - EQ 6.25MG BASE
USFDA APPLICATION NUMBER - 22271
Related Excipient Companies
Rochem International Inc
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ABOUT THIS PAGE
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PharmaCompass offers a list of Alogliptin Benzoate 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 Alogliptin Benzoate manufacturer or Alogliptin Benzoate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Alogliptin Benzoate manufacturer or Alogliptin Benzoate supplier.
PharmaCompass also assists you with knowing the Alogliptin Benzoate API Price utilized in the formulation of products. Alogliptin Benzoate API Price is not always fixed or binding as the Alogliptin Benzoate Price is obtained through a variety of data sources. The Alogliptin Benzoate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A nesina manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of nesina, including repackagers and relabelers. The FDA regulates nesina manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. nesina 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 nesina manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A nesina supplier is an individual or a company that provides nesina active pharmaceutical ingredient (API) or nesina finished formulations upon request. The nesina suppliers may include nesina API manufacturers, exporters, distributors and traders.
click here to find a list of nesina suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A nesina DMF (Drug Master File) is a document detailing the whole manufacturing process of nesina active pharmaceutical ingredient (API) in detail. Different forms of nesina DMFs exist exist since differing nations have different regulations, such as nesina USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A nesina DMF submitted to regulatory agencies in the US is known as a USDMF. nesina USDMF includes data on nesina's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The nesina USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of nesina 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 nesina Drug Master File in Japan (nesina JDMF) empowers nesina 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 nesina JDMF during the approval evaluation for pharmaceutical products. At the time of nesina 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 nesina 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 nesina Drug Master File in Korea (nesina KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of nesina. The MFDS reviews the nesina KDMF as part of the drug registration process and uses the information provided in the nesina KDMF to evaluate the safety and efficacy of the drug.
After submitting a nesina 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 nesina API can apply through the Korea Drug Master File (KDMF).
click here to find a list of nesina suppliers with KDMF on PharmaCompass.
A nesina written confirmation (nesina WC) is an official document issued by a regulatory agency to a nesina manufacturer, verifying that the manufacturing facility of a nesina active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting nesina APIs or nesina finished pharmaceutical products to another nation, regulatory agencies frequently require a nesina WC (written confirmation) as part of the regulatory process.
click here to find a list of nesina 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 nesina as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for nesina 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 nesina 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 nesina and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a nesina NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of nesina suppliers with NDC on PharmaCompass.
nesina 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 nesina 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 nesina GMP manufacturer or nesina GMP API supplier for your needs.
A nesina CoA (Certificate of Analysis) is a formal document that attests to nesina's compliance with nesina specifications and serves as a tool for batch-level quality control.
nesina CoA mostly includes findings from lab analyses of a specific batch. For each nesina 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.
nesina may be tested according to a variety of international standards, such as European Pharmacopoeia (nesina EP), nesina JP (Japanese Pharmacopeia) and the US Pharmacopoeia (nesina USP).
