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