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