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ANALYTICAL
ABOUT THIS PAGE
A Chlorpropamide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Chlorpropamide, including repackagers and relabelers. The FDA regulates Chlorpropamide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Chlorpropamide 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 Chlorpropamide manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Chlorpropamide supplier is an individual or a company that provides Chlorpropamide active pharmaceutical ingredient (API) or Chlorpropamide finished formulations upon request. The Chlorpropamide suppliers may include Chlorpropamide API manufacturers, exporters, distributors and traders.
click here to find a list of Chlorpropamide suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Chlorpropamide DMF (Drug Master File) is a document detailing the whole manufacturing process of Chlorpropamide active pharmaceutical ingredient (API) in detail. Different forms of Chlorpropamide DMFs exist exist since differing nations have different regulations, such as Chlorpropamide USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Chlorpropamide DMF submitted to regulatory agencies in the US is known as a USDMF. Chlorpropamide USDMF includes data on Chlorpropamide's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Chlorpropamide USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Chlorpropamide 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 Chlorpropamide Drug Master File in Japan (Chlorpropamide JDMF) empowers Chlorpropamide 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 Chlorpropamide JDMF during the approval evaluation for pharmaceutical products. At the time of Chlorpropamide 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 Chlorpropamide suppliers with JDMF on PharmaCompass.
A Chlorpropamide CEP of the European Pharmacopoeia monograph is often referred to as a Chlorpropamide Certificate of Suitability (COS). The purpose of a Chlorpropamide CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Chlorpropamide EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Chlorpropamide to their clients by showing that a Chlorpropamide CEP has been issued for it. The manufacturer submits a Chlorpropamide CEP (COS) as part of the market authorization procedure, and it takes on the role of a Chlorpropamide CEP holder for the record. Additionally, the data presented in the Chlorpropamide CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Chlorpropamide DMF.
A Chlorpropamide CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Chlorpropamide 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 Chlorpropamide suppliers with CEP (COS) 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 Chlorpropamide as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Chlorpropamide 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 Chlorpropamide 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 Chlorpropamide and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Chlorpropamide NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Chlorpropamide suppliers with NDC on PharmaCompass.
Chlorpropamide 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 Chlorpropamide 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 Chlorpropamide GMP manufacturer or Chlorpropamide GMP API supplier for your needs.
A Chlorpropamide CoA (Certificate of Analysis) is a formal document that attests to Chlorpropamide's compliance with Chlorpropamide specifications and serves as a tool for batch-level quality control.
Chlorpropamide CoA mostly includes findings from lab analyses of a specific batch. For each Chlorpropamide 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.
Chlorpropamide may be tested according to a variety of international standards, such as European Pharmacopoeia (Chlorpropamide EP), Chlorpropamide JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Chlorpropamide USP).
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