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API SUPPLIERS
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USDMF
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SPI Pharma
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REF. STANDARDS & IMPURITIES
ABOUT THIS PAGE
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PharmaCompass offers a list of Prochlorperazine Maleate 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 Prochlorperazine Maleate manufacturer or Prochlorperazine Maleate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Prochlorperazine Maleate manufacturer or Prochlorperazine Maleate supplier.
PharmaCompass also assists you with knowing the Prochlorperazine Maleate API Price utilized in the formulation of products. Prochlorperazine Maleate API Price is not always fixed or binding as the Prochlorperazine Maleate Price is obtained through a variety of data sources. The Prochlorperazine Maleate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Compazine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Compazine, including repackagers and relabelers. The FDA regulates Compazine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Compazine 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 Compazine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Compazine supplier is an individual or a company that provides Compazine active pharmaceutical ingredient (API) or Compazine finished formulations upon request. The Compazine suppliers may include Compazine API manufacturers, exporters, distributors and traders.
click here to find a list of Compazine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Compazine DMF (Drug Master File) is a document detailing the whole manufacturing process of Compazine active pharmaceutical ingredient (API) in detail. Different forms of Compazine DMFs exist exist since differing nations have different regulations, such as Compazine USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Compazine DMF submitted to regulatory agencies in the US is known as a USDMF. Compazine USDMF includes data on Compazine's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Compazine USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Compazine suppliers with USDMF on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The Compazine Drug Master File in Japan (Compazine JDMF) empowers Compazine API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the Compazine JDMF during the approval evaluation for pharmaceutical products. At the time of Compazine JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Compazine suppliers with JDMF on PharmaCompass.
A Compazine CEP of the European Pharmacopoeia monograph is often referred to as a Compazine Certificate of Suitability (COS). The purpose of a Compazine CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Compazine EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Compazine to their clients by showing that a Compazine CEP has been issued for it. The manufacturer submits a Compazine CEP (COS) as part of the market authorization procedure, and it takes on the role of a Compazine CEP holder for the record. Additionally, the data presented in the Compazine CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Compazine DMF.
A Compazine CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Compazine 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 Compazine suppliers with CEP (COS) on PharmaCompass.
A Compazine written confirmation (Compazine WC) is an official document issued by a regulatory agency to a Compazine manufacturer, verifying that the manufacturing facility of a Compazine active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Compazine APIs or Compazine finished pharmaceutical products to another nation, regulatory agencies frequently require a Compazine WC (written confirmation) as part of the regulatory process.
click here to find a list of Compazine 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 Compazine as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Compazine 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 Compazine 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 Compazine and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Compazine NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Compazine suppliers with NDC on PharmaCompass.
Compazine 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 Compazine 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 Compazine GMP manufacturer or Compazine GMP API supplier for your needs.
A Compazine CoA (Certificate of Analysis) is a formal document that attests to Compazine's compliance with Compazine specifications and serves as a tool for batch-level quality control.
Compazine CoA mostly includes findings from lab analyses of a specific batch. For each Compazine 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.
Compazine may be tested according to a variety of international standards, such as European Pharmacopoeia (Compazine EP), Compazine JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Compazine USP).
