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