Synopsis
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USDMF
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CEP/COS
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JDMF
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EU WC
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KDMF
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FDA Orange Book
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Europe
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Australia
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South Africa
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Listed Dossiers
DRUG PRODUCT COMPOSITIONS
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US Patents
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US Exclusivities
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Health Canada Patents
US Medicaid
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Annual Reports
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Regulatory FDF Prices
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API
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FDF
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Data Compilation #PharmaFlow
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Stock Recap #PipelineProspector
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Weekly News Recap #Phispers
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News #PharmaBuzz
API SUPPLIERS
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FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Microlex e.U
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FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Sigachi Industries
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Fillers, Diluents & Binders
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REF. STANDARDS & IMPURITIES
ABOUT THIS PAGE
56
PharmaCompass offers a list of Deracoxib 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 Deracoxib manufacturer or Deracoxib supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Deracoxib manufacturer or Deracoxib supplier.
PharmaCompass also assists you with knowing the Deracoxib API Price utilized in the formulation of products. Deracoxib API Price is not always fixed or binding as the Deracoxib Price is obtained through a variety of data sources. The Deracoxib Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Deramaxx manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Deramaxx, including repackagers and relabelers. The FDA regulates Deramaxx manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Deramaxx 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 Deramaxx manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Deramaxx supplier is an individual or a company that provides Deramaxx active pharmaceutical ingredient (API) or Deramaxx finished formulations upon request. The Deramaxx suppliers may include Deramaxx API manufacturers, exporters, distributors and traders.
click here to find a list of Deramaxx suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information 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 Deramaxx as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Deramaxx 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 Deramaxx 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 Deramaxx and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Deramaxx NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Deramaxx suppliers with NDC on PharmaCompass.
Deramaxx 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 Deramaxx 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 Deramaxx GMP manufacturer or Deramaxx GMP API supplier for your needs.
A Deramaxx CoA (Certificate of Analysis) is a formal document that attests to Deramaxx's compliance with Deramaxx specifications and serves as a tool for batch-level quality control.
Deramaxx CoA mostly includes findings from lab analyses of a specific batch. For each Deramaxx 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.
Deramaxx may be tested according to a variety of international standards, such as European Pharmacopoeia (Deramaxx EP), Deramaxx JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Deramaxx USP).
