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PharmaCompass offers a list of Aluminum 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 Aluminum manufacturer or Aluminum supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Aluminum manufacturer or Aluminum supplier.
PharmaCompass also assists you with knowing the Aluminum API Price utilized in the formulation of products. Aluminum API Price is not always fixed or binding as the Aluminum Price is obtained through a variety of data sources. The Aluminum Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Aluminium bronze manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Aluminium bronze, including repackagers and relabelers. The FDA regulates Aluminium bronze manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Aluminium bronze 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 Aluminium bronze supplier is an individual or a company that provides Aluminium bronze active pharmaceutical ingredient (API) or Aluminium bronze finished formulations upon request. The Aluminium bronze suppliers may include Aluminium bronze API manufacturers, exporters, distributors and traders.
click here to find a list of Aluminium bronze suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Aluminium bronze CEP of the European Pharmacopoeia monograph is often referred to as a Aluminium bronze Certificate of Suitability (COS). The purpose of a Aluminium bronze CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Aluminium bronze EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Aluminium bronze to their clients by showing that a Aluminium bronze CEP has been issued for it. The manufacturer submits a Aluminium bronze CEP (COS) as part of the market authorization procedure, and it takes on the role of a Aluminium bronze CEP holder for the record. Additionally, the data presented in the Aluminium bronze CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Aluminium bronze DMF.
A Aluminium bronze CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Aluminium bronze 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 Aluminium bronze suppliers with CEP (COS) 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 Aluminium bronze as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Aluminium bronze 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 Aluminium bronze 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 Aluminium bronze and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Aluminium bronze NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Aluminium bronze suppliers with NDC on PharmaCompass.
Aluminium bronze 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 Aluminium bronze 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 Aluminium bronze GMP manufacturer or Aluminium bronze GMP API supplier for your needs.
A Aluminium bronze CoA (Certificate of Analysis) is a formal document that attests to Aluminium bronze's compliance with Aluminium bronze specifications and serves as a tool for batch-level quality control.
Aluminium bronze CoA mostly includes findings from lab analyses of a specific batch. For each Aluminium bronze 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.
Aluminium bronze may be tested according to a variety of international standards, such as European Pharmacopoeia (Aluminium bronze EP), Aluminium bronze JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Aluminium bronze USP).