API Suppliers
US DMFs Filed
CEP/COS Certifications
JDMFs Filed
0
EU WC
Listed Suppliers
USA (Orange Book)
Europe
Canada
Australia
South Africa
Uploaded Dossiers
U.S. Medicaid
Annual Reports
0
68
PharmaCompass offers a list of Albendazole 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 Albendazole manufacturer or Albendazole supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Albendazole manufacturer or Albendazole supplier.
PharmaCompass also assists you with knowing the Albendazole API Price utilized in the formulation of products. Albendazole API Price is not always fixed or binding as the Albendazole Price is obtained through a variety of data sources. The Albendazole Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Albendazole manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Albendazole, including repackagers and relabelers. The FDA regulates Albendazole manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Albendazole 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 Albendazole manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Albendazole supplier is an individual or a company that provides Albendazole active pharmaceutical ingredient (API) or Albendazole finished formulations upon request. The Albendazole suppliers may include Albendazole API manufacturers, exporters, distributors and traders.
click here to find a list of Albendazole suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Albendazole DMF (Drug Master File) is a document detailing the whole manufacturing process of Albendazole active pharmaceutical ingredient (API) in detail. Different forms of Albendazole DMFs exist exist since differing nations have different regulations, such as Albendazole USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Albendazole DMF submitted to regulatory agencies in the US is known as a USDMF. Albendazole USDMF includes data on Albendazole's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Albendazole USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Albendazole suppliers with USDMF on PharmaCompass.
A Albendazole CEP of the European Pharmacopoeia monograph is often referred to as a Albendazole Certificate of Suitability (COS). The purpose of a Albendazole CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Albendazole EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Albendazole to their clients by showing that a Albendazole CEP has been issued for it. The manufacturer submits a Albendazole CEP (COS) as part of the market authorization procedure, and it takes on the role of a Albendazole CEP holder for the record. Additionally, the data presented in the Albendazole CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Albendazole DMF.
A Albendazole CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Albendazole 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 Albendazole suppliers with CEP (COS) on PharmaCompass.
A Albendazole written confirmation (Albendazole WC) is an official document issued by a regulatory agency to a Albendazole manufacturer, verifying that the manufacturing facility of a Albendazole active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Albendazole APIs or Albendazole finished pharmaceutical products to another nation, regulatory agencies frequently require a Albendazole WC (written confirmation) as part of the regulatory process.
click here to find a list of Albendazole 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 Albendazole as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Albendazole 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 Albendazole 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 Albendazole and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Albendazole NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Albendazole suppliers with NDC on PharmaCompass.
Albendazole 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 Albendazole 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 Albendazole GMP manufacturer or Albendazole GMP API supplier for your needs.
A Albendazole CoA (Certificate of Analysis) is a formal document that attests to Albendazole's compliance with Albendazole specifications and serves as a tool for batch-level quality control.
Albendazole CoA mostly includes findings from lab analyses of a specific batch. For each Albendazole 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.
Albendazole may be tested according to a variety of international standards, such as European Pharmacopoeia (Albendazole EP), Albendazole JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Albendazole USP).