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1. (2r)-2-hydroxy-2-(nitromethyl)butanedioic Acid
2. Q27463937
Molecular Weight | 193.11 g/mol |
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Molecular Formula | C5H7NO7 |
XLogP3 | -1.4 |
Hydrogen Bond Donor Count | 3 |
Hydrogen Bond Acceptor Count | 7 |
Rotatable Bond Count | 4 |
Exact Mass | 193.02225156 g/mol |
Monoisotopic Mass | 193.02225156 g/mol |
Topological Polar Surface Area | 141 Ų |
Heavy Atom Count | 13 |
Formal Charge | 0 |
Complexity | 244 |
Isotope Atom Count | 0 |
Defined Atom Stereocenter Count | 1 |
Undefined Atom Stereocenter Count | 0 |
Defined Bond Stereocenter Count | 0 |
Undefined Bond Stereocenter Count | 0 |
Covalently Bonded Unit Count | 1 |
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PharmaCompass offers a list of Ntc 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 Ntc manufacturer or Ntc supplier for your needs.
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PharmaCompass also assists you with knowing the Ntc API Price utilized in the formulation of products. Ntc API Price is not always fixed or binding as the Ntc Price is obtained through a variety of data sources. The Ntc Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A NTC-801F manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of NTC-801F, including repackagers and relabelers. The FDA regulates NTC-801F manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. NTC-801F 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 NTC-801F supplier is an individual or a company that provides NTC-801F active pharmaceutical ingredient (API) or NTC-801F finished formulations upon request. The NTC-801F suppliers may include NTC-801F API manufacturers, exporters, distributors and traders.
click here to find a list of NTC-801F suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A NTC-801F DMF (Drug Master File) is a document detailing the whole manufacturing process of NTC-801F active pharmaceutical ingredient (API) in detail. Different forms of NTC-801F DMFs exist exist since differing nations have different regulations, such as NTC-801F USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A NTC-801F DMF submitted to regulatory agencies in the US is known as a USDMF. NTC-801F USDMF includes data on NTC-801F's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The NTC-801F USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of NTC-801F suppliers with USDMF on PharmaCompass.
NTC-801F 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 NTC-801F 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 NTC-801F GMP manufacturer or NTC-801F GMP API supplier for your needs.
A NTC-801F CoA (Certificate of Analysis) is a formal document that attests to NTC-801F's compliance with NTC-801F specifications and serves as a tool for batch-level quality control.
NTC-801F CoA mostly includes findings from lab analyses of a specific batch. For each NTC-801F 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.
NTC-801F may be tested according to a variety of international standards, such as European Pharmacopoeia (NTC-801F EP), NTC-801F JP (Japanese Pharmacopeia) and the US Pharmacopoeia (NTC-801F USP).