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1. 189032-40-4
2. Unii-el5u85ukd2
3. Nesiritide Citrate [usan]
4. El5u85ukd2
5. Natriuretic Factor-32 (human Brain Clone Lambdahbnp57), 2-hydroxy-1,2,3-propanetricarboxylate (salt)
6. Brain Natriuretic Peptide-32 (human), 2-hydroxy-1,2,3-propanetricarboxylate (salt)
7. L-seryl-l-prolyl-l-lysyl-l-methionyl-l-valyl-l-glutaminylglycyl-l-serylglycyl-l-cysteinyl-l-phenylalanylglycyl-l-arginyl-l-lysyl-l-methionyl-l-aspartyl-l-arginyl-l-isoleucyl-l-seryl-l-seryl-l-seryl-l-serylglycyl-l-leucylglycyl-l-cysteinyl-l-lysyl-l-valyl-l-leucyl-l-arginyl-l-arginyl-l-histidine Cyclic(10-26) - Disulfide Citrate (salt)
Molecular Weight | 3656.2 g/mol |
---|---|
Molecular Formula | C149H252N50O49S4 |
Hydrogen Bond Donor Count | 60 |
Hydrogen Bond Acceptor Count | 62 |
Rotatable Bond Count | 96 |
Exact Mass | 3654.7680641 g/mol |
Monoisotopic Mass | 3653.7647093 g/mol |
Topological Polar Surface Area | 1750 Ų |
Heavy Atom Count | 252 |
Formal Charge | 0 |
Complexity | 7970 |
Isotope Atom Count | 0 |
Defined Atom Stereocenter Count | 28 |
Undefined Atom Stereocenter Count | 0 |
Defined Bond Stereocenter Count | 0 |
Undefined Bond Stereocenter Count | 0 |
Covalently Bonded Unit Count | 2 |
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ABOUT THIS PAGE
A Natriuretic Peptide, Brain manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Natriuretic Peptide, Brain, including repackagers and relabelers. The FDA regulates Natriuretic Peptide, Brain manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Natriuretic Peptide, Brain 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 Natriuretic Peptide, Brain manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Natriuretic Peptide, Brain supplier is an individual or a company that provides Natriuretic Peptide, Brain active pharmaceutical ingredient (API) or Natriuretic Peptide, Brain finished formulations upon request. The Natriuretic Peptide, Brain suppliers may include Natriuretic Peptide, Brain API manufacturers, exporters, distributors and traders.
click here to find a list of Natriuretic Peptide, Brain suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Natriuretic Peptide, Brain DMF (Drug Master File) is a document detailing the whole manufacturing process of Natriuretic Peptide, Brain active pharmaceutical ingredient (API) in detail. Different forms of Natriuretic Peptide, Brain DMFs exist exist since differing nations have different regulations, such as Natriuretic Peptide, Brain USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Natriuretic Peptide, Brain DMF submitted to regulatory agencies in the US is known as a USDMF. Natriuretic Peptide, Brain USDMF includes data on Natriuretic Peptide, Brain's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Natriuretic Peptide, Brain USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Natriuretic Peptide, Brain 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 Natriuretic Peptide, Brain as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Natriuretic Peptide, Brain 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 Natriuretic Peptide, Brain 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 Natriuretic Peptide, Brain and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Natriuretic Peptide, Brain NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Natriuretic Peptide, Brain suppliers with NDC on PharmaCompass.
Natriuretic Peptide, Brain 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 Natriuretic Peptide, Brain 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 Natriuretic Peptide, Brain GMP manufacturer or Natriuretic Peptide, Brain GMP API supplier for your needs.
A Natriuretic Peptide, Brain CoA (Certificate of Analysis) is a formal document that attests to Natriuretic Peptide, Brain's compliance with Natriuretic Peptide, Brain specifications and serves as a tool for batch-level quality control.
Natriuretic Peptide, Brain CoA mostly includes findings from lab analyses of a specific batch. For each Natriuretic Peptide, Brain 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.
Natriuretic Peptide, Brain may be tested according to a variety of international standards, such as European Pharmacopoeia (Natriuretic Peptide, Brain EP), Natriuretic Peptide, Brain JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Natriuretic Peptide, Brain USP).
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