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