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