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