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API SUPPLIERS
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USDMF
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DOSAGE - CAPSULE, DELAYED RELEASE;ORAL - EQ 2...DOSAGE - CAPSULE, DELAYED RELEASE;ORAL - EQ 20MG BASE
USFDA APPLICATION NUMBER - 204655
DOSAGE - CAPSULE, DELAYED REL PELLETS;ORAL - ...DOSAGE - CAPSULE, DELAYED REL PELLETS;ORAL - EQ 20MG BASE
USFDA APPLICATION NUMBER - 21153
DOSAGE - CAPSULE, DELAYED REL PELLETS;ORAL - ...DOSAGE - CAPSULE, DELAYED REL PELLETS;ORAL - EQ 40MG BASE
USFDA APPLICATION NUMBER - 21153
DOSAGE - FOR SUSPENSION, DELAYED RELEASE;ORAL...DOSAGE - FOR SUSPENSION, DELAYED RELEASE;ORAL - EQ 2.5MG BASE/PACKET
USFDA APPLICATION NUMBER - 21957
DOSAGE - FOR SUSPENSION, DELAYED RELEASE;ORAL...DOSAGE - FOR SUSPENSION, DELAYED RELEASE;ORAL - EQ 20MG BASE/PACKET
USFDA APPLICATION NUMBER - 21957
DOSAGE - FOR SUSPENSION, DELAYED RELEASE;ORAL...DOSAGE - FOR SUSPENSION, DELAYED RELEASE;ORAL - EQ 40MG BASE/PACKET
USFDA APPLICATION NUMBER - 21957
DOSAGE - FOR SUSPENSION, DELAYED RELEASE;ORAL...DOSAGE - FOR SUSPENSION, DELAYED RELEASE;ORAL - EQ 5MG BASE/PACKET
USFDA APPLICATION NUMBER - 21957
DOSAGE - TABLET, DELAYED RELEASE;ORAL - EQ 20...DOSAGE - TABLET, DELAYED RELEASE;ORAL - EQ 20MG BASE;375MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
USFDA APPLICATION NUMBER - 22511
DOSAGE - TABLET, DELAYED RELEASE;ORAL - EQ 20...DOSAGE - TABLET, DELAYED RELEASE;ORAL - EQ 20MG BASE;500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
USFDA APPLICATION NUMBER - 22511
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ABOUT THIS PAGE
15
PharmaCompass offers a list of Esomeprazole Magnesium 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 Esomeprazole Magnesium manufacturer or Esomeprazole Magnesium supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Esomeprazole Magnesium manufacturer or Esomeprazole Magnesium supplier.
PharmaCompass also assists you with knowing the Esomeprazole Magnesium API Price utilized in the formulation of products. Esomeprazole Magnesium API Price is not always fixed or binding as the Esomeprazole Magnesium Price is obtained through a variety of data sources. The Esomeprazole Magnesium Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Nexium, Esomeprazole magnesium manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Nexium, Esomeprazole magnesium, including repackagers and relabelers. The FDA regulates Nexium, Esomeprazole magnesium manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Nexium, Esomeprazole magnesium 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 Nexium, Esomeprazole magnesium manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Nexium, Esomeprazole magnesium supplier is an individual or a company that provides Nexium, Esomeprazole magnesium active pharmaceutical ingredient (API) or Nexium, Esomeprazole magnesium finished formulations upon request. The Nexium, Esomeprazole magnesium suppliers may include Nexium, Esomeprazole magnesium API manufacturers, exporters, distributors and traders.
click here to find a list of Nexium, Esomeprazole magnesium suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Nexium, Esomeprazole magnesium DMF (Drug Master File) is a document detailing the whole manufacturing process of Nexium, Esomeprazole magnesium active pharmaceutical ingredient (API) in detail. Different forms of Nexium, Esomeprazole magnesium DMFs exist exist since differing nations have different regulations, such as Nexium, Esomeprazole magnesium USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Nexium, Esomeprazole magnesium DMF submitted to regulatory agencies in the US is known as a USDMF. Nexium, Esomeprazole magnesium USDMF includes data on Nexium, Esomeprazole magnesium's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Nexium, Esomeprazole magnesium USDMF is kept confidential to protect the manufacturer’s intellectual property.
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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 Nexium, Esomeprazole magnesium Drug Master File in Japan (Nexium, Esomeprazole magnesium JDMF) empowers Nexium, Esomeprazole magnesium 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 Nexium, Esomeprazole magnesium JDMF during the approval evaluation for pharmaceutical products. At the time of Nexium, Esomeprazole magnesium 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 Nexium, Esomeprazole magnesium 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 Nexium, Esomeprazole magnesium Drug Master File in Korea (Nexium, Esomeprazole magnesium KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Nexium, Esomeprazole magnesium. The MFDS reviews the Nexium, Esomeprazole magnesium KDMF as part of the drug registration process and uses the information provided in the Nexium, Esomeprazole magnesium KDMF to evaluate the safety and efficacy of the drug.
After submitting a Nexium, Esomeprazole magnesium 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 Nexium, Esomeprazole magnesium API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Nexium, Esomeprazole magnesium suppliers with KDMF on PharmaCompass.
A Nexium, Esomeprazole magnesium CEP of the European Pharmacopoeia monograph is often referred to as a Nexium, Esomeprazole magnesium Certificate of Suitability (COS). The purpose of a Nexium, Esomeprazole magnesium CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Nexium, Esomeprazole magnesium EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Nexium, Esomeprazole magnesium to their clients by showing that a Nexium, Esomeprazole magnesium CEP has been issued for it. The manufacturer submits a Nexium, Esomeprazole magnesium CEP (COS) as part of the market authorization procedure, and it takes on the role of a Nexium, Esomeprazole magnesium CEP holder for the record. Additionally, the data presented in the Nexium, Esomeprazole magnesium CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Nexium, Esomeprazole magnesium DMF.
A Nexium, Esomeprazole magnesium CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Nexium, Esomeprazole magnesium 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 Nexium, Esomeprazole magnesium suppliers with CEP (COS) on PharmaCompass.
A Nexium, Esomeprazole magnesium written confirmation (Nexium, Esomeprazole magnesium WC) is an official document issued by a regulatory agency to a Nexium, Esomeprazole magnesium manufacturer, verifying that the manufacturing facility of a Nexium, Esomeprazole magnesium active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Nexium, Esomeprazole magnesium APIs or Nexium, Esomeprazole magnesium finished pharmaceutical products to another nation, regulatory agencies frequently require a Nexium, Esomeprazole magnesium WC (written confirmation) as part of the regulatory process.
click here to find a list of Nexium, Esomeprazole magnesium 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 Nexium, Esomeprazole magnesium as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Nexium, Esomeprazole magnesium 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 Nexium, Esomeprazole magnesium 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 Nexium, Esomeprazole magnesium and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Nexium, Esomeprazole magnesium NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Nexium, Esomeprazole magnesium suppliers with NDC on PharmaCompass.
Nexium, Esomeprazole magnesium 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 Nexium, Esomeprazole magnesium 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 Nexium, Esomeprazole magnesium GMP manufacturer or Nexium, Esomeprazole magnesium GMP API supplier for your needs.
A Nexium, Esomeprazole magnesium CoA (Certificate of Analysis) is a formal document that attests to Nexium, Esomeprazole magnesium's compliance with Nexium, Esomeprazole magnesium specifications and serves as a tool for batch-level quality control.
Nexium, Esomeprazole magnesium CoA mostly includes findings from lab analyses of a specific batch. For each Nexium, Esomeprazole magnesium 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.
Nexium, Esomeprazole magnesium may be tested according to a variety of international standards, such as European Pharmacopoeia (Nexium, Esomeprazole magnesium EP), Nexium, Esomeprazole magnesium JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Nexium, Esomeprazole magnesium USP).
