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