Synopsis
0
CEP/COS
0
KDMF
0
VMF
0
EDQM
0
USP
0
JP
0
Others
0
Europe
0
Canada
0
Australia
0
South Africa
0
Listed Dossiers
DRUG PRODUCT COMPOSITIONS
0
US Patents
0
US Exclusivities
0
Health Canada Patents
US Medicaid
NA
Annual Reports
NA
Regulatory FDF Prices
NA
0
API
0
FDF
0
Data Compilation #PharmaFlow
0
Stock Recap #PipelineProspector
0
Weekly News Recap #Phispers
API SUPPLIERS
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]
USDMF
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]EU WC
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Related Excipient Companies
Digital Content
NEWS #PharmaBuzz
ABOUT THIS PAGE
36
PharmaCompass offers a list of Indomethacin Sodium 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 Indomethacin Sodium manufacturer or Indomethacin Sodium supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Indomethacin Sodium manufacturer or Indomethacin Sodium supplier.
PharmaCompass also assists you with knowing the Indomethacin Sodium API Price utilized in the formulation of products. Indomethacin Sodium API Price is not always fixed or binding as the Indomethacin Sodium Price is obtained through a variety of data sources. The Indomethacin Sodium Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Sodium Indomethacin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sodium Indomethacin, including repackagers and relabelers. The FDA regulates Sodium Indomethacin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sodium Indomethacin 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 Sodium Indomethacin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Sodium Indomethacin supplier is an individual or a company that provides Sodium Indomethacin active pharmaceutical ingredient (API) or Sodium Indomethacin finished formulations upon request. The Sodium Indomethacin suppliers may include Sodium Indomethacin API manufacturers, exporters, distributors and traders.
click here to find a list of Sodium Indomethacin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Sodium Indomethacin DMF (Drug Master File) is a document detailing the whole manufacturing process of Sodium Indomethacin active pharmaceutical ingredient (API) in detail. Different forms of Sodium Indomethacin DMFs exist exist since differing nations have different regulations, such as Sodium Indomethacin USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Sodium Indomethacin DMF submitted to regulatory agencies in the US is known as a USDMF. Sodium Indomethacin USDMF includes data on Sodium Indomethacin's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Sodium Indomethacin USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Sodium Indomethacin 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 Sodium Indomethacin Drug Master File in Japan (Sodium Indomethacin JDMF) empowers Sodium Indomethacin 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 Sodium Indomethacin JDMF during the approval evaluation for pharmaceutical products. At the time of Sodium Indomethacin 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 Sodium Indomethacin suppliers with JDMF on PharmaCompass.
A Sodium Indomethacin written confirmation (Sodium Indomethacin WC) is an official document issued by a regulatory agency to a Sodium Indomethacin manufacturer, verifying that the manufacturing facility of a Sodium Indomethacin active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Sodium Indomethacin APIs or Sodium Indomethacin finished pharmaceutical products to another nation, regulatory agencies frequently require a Sodium Indomethacin WC (written confirmation) as part of the regulatory process.
click here to find a list of Sodium Indomethacin 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 Sodium Indomethacin as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Sodium Indomethacin 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 Sodium Indomethacin 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 Sodium Indomethacin and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Sodium Indomethacin NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Sodium Indomethacin suppliers with NDC on PharmaCompass.
Sodium Indomethacin 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 Sodium Indomethacin 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 Sodium Indomethacin GMP manufacturer or Sodium Indomethacin GMP API supplier for your needs.
A Sodium Indomethacin CoA (Certificate of Analysis) is a formal document that attests to Sodium Indomethacin's compliance with Sodium Indomethacin specifications and serves as a tool for batch-level quality control.
Sodium Indomethacin CoA mostly includes findings from lab analyses of a specific batch. For each Sodium Indomethacin 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.
Sodium Indomethacin may be tested according to a variety of international standards, such as European Pharmacopoeia (Sodium Indomethacin EP), Sodium Indomethacin JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Sodium Indomethacin USP).
