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API SUPPLIERS
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USDMF
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DOSAGE - TABLET;ORAL - EQ 40MG MEDOXOMIL
USFDA APPLICATION NUMBER - 200796
DOSAGE - TABLET;ORAL - EQ 80MG MEDOXOMIL
USFDA APPLICATION NUMBER - 200796
DOSAGE - TABLET;ORAL - EQ 40MG MEDOXOMIL;12.5...DOSAGE - TABLET;ORAL - EQ 40MG MEDOXOMIL;12.5MG
USFDA APPLICATION NUMBER - 202331
DOSAGE - TABLET;ORAL - EQ 40MG MEDOXOMIL;25MG
USFDA APPLICATION NUMBER - 202331
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REF. STANDARDS & IMPURITIES
ABOUT THIS PAGE
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PharmaCompass offers a list of Azilsartan 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 Azilsartan manufacturer or Azilsartan supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Azilsartan manufacturer or Azilsartan supplier.
PharmaCompass also assists you with knowing the Azilsartan API Price utilized in the formulation of products. Azilsartan API Price is not always fixed or binding as the Azilsartan Price is obtained through a variety of data sources. The Azilsartan Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Edarbi manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Edarbi, including repackagers and relabelers. The FDA regulates Edarbi manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Edarbi 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 Edarbi manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Edarbi supplier is an individual or a company that provides Edarbi active pharmaceutical ingredient (API) or Edarbi finished formulations upon request. The Edarbi suppliers may include Edarbi API manufacturers, exporters, distributors and traders.
click here to find a list of Edarbi suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Edarbi DMF (Drug Master File) is a document detailing the whole manufacturing process of Edarbi active pharmaceutical ingredient (API) in detail. Different forms of Edarbi DMFs exist exist since differing nations have different regulations, such as Edarbi USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Edarbi DMF submitted to regulatory agencies in the US is known as a USDMF. Edarbi USDMF includes data on Edarbi's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Edarbi USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Edarbi 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 Edarbi Drug Master File in Japan (Edarbi JDMF) empowers Edarbi 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 Edarbi JDMF during the approval evaluation for pharmaceutical products. At the time of Edarbi 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 Edarbi 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 Edarbi Drug Master File in Korea (Edarbi KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Edarbi. The MFDS reviews the Edarbi KDMF as part of the drug registration process and uses the information provided in the Edarbi KDMF to evaluate the safety and efficacy of the drug.
After submitting a Edarbi 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 Edarbi API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Edarbi suppliers with KDMF on PharmaCompass.
A Edarbi written confirmation (Edarbi WC) is an official document issued by a regulatory agency to a Edarbi manufacturer, verifying that the manufacturing facility of a Edarbi active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Edarbi APIs or Edarbi finished pharmaceutical products to another nation, regulatory agencies frequently require a Edarbi WC (written confirmation) as part of the regulatory process.
click here to find a list of Edarbi 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 Edarbi as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Edarbi 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 Edarbi 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 Edarbi and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Edarbi NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Edarbi suppliers with NDC on PharmaCompass.
Edarbi 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 Edarbi 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 Edarbi GMP manufacturer or Edarbi GMP API supplier for your needs.
A Edarbi CoA (Certificate of Analysis) is a formal document that attests to Edarbi's compliance with Edarbi specifications and serves as a tool for batch-level quality control.
Edarbi CoA mostly includes findings from lab analyses of a specific batch. For each Edarbi 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.
Edarbi may be tested according to a variety of international standards, such as European Pharmacopoeia (Edarbi EP), Edarbi JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Edarbi USP).
