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API SUPPLIERS
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PharmaCompass offers a list of Hydrotalcite 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 Hydrotalcite manufacturer or Hydrotalcite supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Hydrotalcite manufacturer or Hydrotalcite supplier.
PharmaCompass also assists you with knowing the Hydrotalcite API Price utilized in the formulation of products. Hydrotalcite API Price is not always fixed or binding as the Hydrotalcite Price is obtained through a variety of data sources. The Hydrotalcite Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Altacet manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Altacet, including repackagers and relabelers. The FDA regulates Altacet manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Altacet API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Altacet supplier is an individual or a company that provides Altacet active pharmaceutical ingredient (API) or Altacet finished formulations upon request. The Altacet suppliers may include Altacet API manufacturers, exporters, distributors and traders.
click here to find a list of Altacet suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Altacet written confirmation (Altacet WC) is an official document issued by a regulatory agency to a Altacet manufacturer, verifying that the manufacturing facility of a Altacet active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Altacet APIs or Altacet finished pharmaceutical products to another nation, regulatory agencies frequently require a Altacet WC (written confirmation) as part of the regulatory process.
click here to find a list of Altacet 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 Altacet as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Altacet 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 Altacet 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 Altacet and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Altacet NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Altacet suppliers with NDC on PharmaCompass.
Altacet 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 Altacet 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 Altacet GMP manufacturer or Altacet GMP API supplier for your needs.
A Altacet CoA (Certificate of Analysis) is a formal document that attests to Altacet's compliance with Altacet specifications and serves as a tool for batch-level quality control.
Altacet CoA mostly includes findings from lab analyses of a specific batch. For each Altacet 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.
Altacet may be tested according to a variety of international standards, such as European Pharmacopoeia (Altacet EP), Altacet JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Altacet USP).
