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