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