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REF. STANDARDS & IMPURITIES
ABOUT THIS PAGE
A Disopyramide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Disopyramide, including repackagers and relabelers. The FDA regulates Disopyramide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Disopyramide 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 Disopyramide manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Disopyramide supplier is an individual or a company that provides Disopyramide active pharmaceutical ingredient (API) or Disopyramide finished formulations upon request. The Disopyramide suppliers may include Disopyramide API manufacturers, exporters, distributors and traders.
click here to find a list of Disopyramide suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Disopyramide DMF (Drug Master File) is a document detailing the whole manufacturing process of Disopyramide active pharmaceutical ingredient (API) in detail. Different forms of Disopyramide DMFs exist exist since differing nations have different regulations, such as Disopyramide USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Disopyramide DMF submitted to regulatory agencies in the US is known as a USDMF. Disopyramide USDMF includes data on Disopyramide's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Disopyramide USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Disopyramide 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 Disopyramide Drug Master File in Japan (Disopyramide JDMF) empowers Disopyramide 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 Disopyramide JDMF during the approval evaluation for pharmaceutical products. At the time of Disopyramide 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 Disopyramide suppliers with JDMF 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 Disopyramide as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Disopyramide 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 Disopyramide 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 Disopyramide and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Disopyramide NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Disopyramide suppliers with NDC on PharmaCompass.
Disopyramide 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 Disopyramide 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 Disopyramide GMP manufacturer or Disopyramide GMP API supplier for your needs.
A Disopyramide CoA (Certificate of Analysis) is a formal document that attests to Disopyramide's compliance with Disopyramide specifications and serves as a tool for batch-level quality control.
Disopyramide CoA mostly includes findings from lab analyses of a specific batch. For each Disopyramide 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.
Disopyramide may be tested according to a variety of international standards, such as European Pharmacopoeia (Disopyramide EP), Disopyramide JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Disopyramide USP).
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