X
API Suppliers
US DMFs Filed
CEP/COS Certifications
0
JDMFs Filed
Other Certificates
0
Other Suppliers
USA (Orange Book)
Europe
Canada
Australia
South Africa
Uploaded Dossiers
0
U.S. Medicaid
Annual Reports
0
73
PharmaCompass offers a list of Disopyramide 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 Disopyramide manufacturer or Disopyramide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Disopyramide manufacturer or Disopyramide supplier.
PharmaCompass also assists you with knowing the Disopyramide API Price utilized in the formulation of products. Disopyramide API Price is not always fixed or binding as the Disopyramide Price is obtained through a variety of data sources. The Disopyramide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Disopyramide Phosphate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Disopyramide Phosphate, including repackagers and relabelers. The FDA regulates Disopyramide Phosphate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Disopyramide Phosphate 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 Phosphate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Disopyramide Phosphate supplier is an individual or a company that provides Disopyramide Phosphate active pharmaceutical ingredient (API) or Disopyramide Phosphate finished formulations upon request. The Disopyramide Phosphate suppliers may include Disopyramide Phosphate API manufacturers, exporters, distributors and traders.
click here to find a list of Disopyramide Phosphate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Disopyramide Phosphate DMF (Drug Master File) is a document detailing the whole manufacturing process of Disopyramide Phosphate active pharmaceutical ingredient (API) in detail. Different forms of Disopyramide Phosphate DMFs exist exist since differing nations have different regulations, such as Disopyramide Phosphate USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Disopyramide Phosphate DMF submitted to regulatory agencies in the US is known as a USDMF. Disopyramide Phosphate USDMF includes data on Disopyramide Phosphate's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Disopyramide Phosphate USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Disopyramide Phosphate 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 Phosphate Drug Master File in Japan (Disopyramide Phosphate JDMF) empowers Disopyramide Phosphate 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 Phosphate JDMF during the approval evaluation for pharmaceutical products. At the time of Disopyramide Phosphate 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 Phosphate 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 Phosphate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Disopyramide Phosphate 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 Phosphate 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 Phosphate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Disopyramide Phosphate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Disopyramide Phosphate suppliers with NDC on PharmaCompass.
Disopyramide Phosphate 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 Phosphate 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 Phosphate GMP manufacturer or Disopyramide Phosphate GMP API supplier for your needs.
A Disopyramide Phosphate CoA (Certificate of Analysis) is a formal document that attests to Disopyramide Phosphate's compliance with Disopyramide Phosphate specifications and serves as a tool for batch-level quality control.
Disopyramide Phosphate CoA mostly includes findings from lab analyses of a specific batch. For each Disopyramide Phosphate 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 Phosphate may be tested according to a variety of international standards, such as European Pharmacopoeia (Disopyramide Phosphate EP), Disopyramide Phosphate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Disopyramide Phosphate USP).
Market Place
