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VMF
DRUG PRODUCT COMPOSITIONS0
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Data Compilation #PharmaFlow
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API SUPPLIERS
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USDMF
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API Imports and Exports
Drugs in Development
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DOSAGE - TABLET;ORAL - 1.25MG
USFDA APPLICATION NUMBER - 17532
DOSAGE - TABLET;ORAL - 2.5MG
USFDA APPLICATION NUMBER - 17532
DOSAGE - TABLET;ORAL - 5MG
USFDA APPLICATION NUMBER - 17532
DOSAGE - TABLET;ORAL - 1.25MG;250MG **Federal...DOSAGE - TABLET;ORAL - 1.25MG;250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
USFDA APPLICATION NUMBER - 21178
DOSAGE - TABLET;ORAL - 2.5MG;500MG **Federal ...DOSAGE - TABLET;ORAL - 2.5MG;500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
USFDA APPLICATION NUMBER - 21178
DOSAGE - TABLET;ORAL - 5MG;500MG **Federal Re...DOSAGE - TABLET;ORAL - 5MG;500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
USFDA APPLICATION NUMBER - 21178
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REF. STANDARDS & IMPURITIES
ABOUT THIS PAGE
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PharmaCompass offers a list of Glibenclamide 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 Glibenclamide manufacturer or Glibenclamide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Glibenclamide manufacturer or Glibenclamide supplier.
PharmaCompass also assists you with knowing the Glibenclamide API Price utilized in the formulation of products. Glibenclamide API Price is not always fixed or binding as the Glibenclamide Price is obtained through a variety of data sources. The Glibenclamide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Glisulin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Glisulin, including repackagers and relabelers. The FDA regulates Glisulin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Glisulin 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 Glisulin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Glisulin supplier is an individual or a company that provides Glisulin active pharmaceutical ingredient (API) or Glisulin finished formulations upon request. The Glisulin suppliers may include Glisulin API manufacturers, exporters, distributors and traders.
click here to find a list of Glisulin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Glisulin DMF (Drug Master File) is a document detailing the whole manufacturing process of Glisulin active pharmaceutical ingredient (API) in detail. Different forms of Glisulin DMFs exist exist since differing nations have different regulations, such as Glisulin USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Glisulin DMF submitted to regulatory agencies in the US is known as a USDMF. Glisulin USDMF includes data on Glisulin's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Glisulin USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Glisulin 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 Glisulin Drug Master File in Japan (Glisulin JDMF) empowers Glisulin 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 Glisulin JDMF during the approval evaluation for pharmaceutical products. At the time of Glisulin 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 Glisulin 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 Glisulin Drug Master File in Korea (Glisulin KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Glisulin. The MFDS reviews the Glisulin KDMF as part of the drug registration process and uses the information provided in the Glisulin KDMF to evaluate the safety and efficacy of the drug.
After submitting a Glisulin 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 Glisulin API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Glisulin suppliers with KDMF on PharmaCompass.
A Glisulin CEP of the European Pharmacopoeia monograph is often referred to as a Glisulin Certificate of Suitability (COS). The purpose of a Glisulin CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Glisulin EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Glisulin to their clients by showing that a Glisulin CEP has been issued for it. The manufacturer submits a Glisulin CEP (COS) as part of the market authorization procedure, and it takes on the role of a Glisulin CEP holder for the record. Additionally, the data presented in the Glisulin CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Glisulin DMF.
A Glisulin CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Glisulin 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 Glisulin suppliers with CEP (COS) on PharmaCompass.
A Glisulin written confirmation (Glisulin WC) is an official document issued by a regulatory agency to a Glisulin manufacturer, verifying that the manufacturing facility of a Glisulin active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Glisulin APIs or Glisulin finished pharmaceutical products to another nation, regulatory agencies frequently require a Glisulin WC (written confirmation) as part of the regulatory process.
click here to find a list of Glisulin 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 Glisulin as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Glisulin 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 Glisulin 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 Glisulin and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Glisulin NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Glisulin suppliers with NDC on PharmaCompass.
Glisulin 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 Glisulin 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 Glisulin GMP manufacturer or Glisulin GMP API supplier for your needs.
A Glisulin CoA (Certificate of Analysis) is a formal document that attests to Glisulin's compliance with Glisulin specifications and serves as a tool for batch-level quality control.
Glisulin CoA mostly includes findings from lab analyses of a specific batch. For each Glisulin 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.
Glisulin may be tested according to a variety of international standards, such as European Pharmacopoeia (Glisulin EP), Glisulin JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Glisulin USP).
