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