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