Synopsis
Synopsis
0
CEP/COS
0
JDMF
0
EU WC
0
KDMF
0
NDC API
0
VMF
0
Listed Suppliers
0
API
0
FDF
0
FDF Dossiers
0
FDA Orange Book
0
Europe
0
Canada
0
Australia
0
South Africa
0
Listed Dossiers
DRUG PRODUCT COMPOSITIONS
0
US Patents
0
US Exclusivities
0
Health Canada Patents
0
Data Compilation #PharmaFlow
0
Stock Recap #PipelineProspector
0
Weekly News Recap #Phispers
US Medicaid
NA
Annual Reports
NA
Finished Drug Prices
NA
1. Chembl4071327
| Molecular Weight | 3464.0 g/mol |
|---|---|
| Molecular Formula | C143H244N50O42S4 |
| XLogP3 | -17.2 |
| Hydrogen Bond Donor Count | 55 |
| Hydrogen Bond Acceptor Count | 55 |
| Rotatable Bond Count | 91 |
| Exact Mass | 3462.7410615 g/mol |
| Monoisotopic Mass | 3461.7377067 g/mol |
| Topological Polar Surface Area | 1610 Ų |
| Heavy Atom Count | 239 |
| Formal Charge | 0 |
| Complexity | 7860 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 28 |
| Undefined Atom Stereocenter Count | 1 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
| 1 of 2 | |
|---|---|
| Drug Name | Natrecor |
| PubMed Health | Nesiritide (Injection) |
| Drug Classes | Antianginal, Cardiovascular Agent |
| Active Ingredient | Nesiritide recombinant |
| Dosage Form | For solution |
| Route | Intravenous |
| Strength | 1.5mg/vial |
| Market Status | Prescription |
| Company | Scios |
| 2 of 2 | |
|---|---|
| Drug Name | Natrecor |
| PubMed Health | Nesiritide (Injection) |
| Drug Classes | Antianginal, Cardiovascular Agent |
| Active Ingredient | Nesiritide recombinant |
| Dosage Form | For solution |
| Route | Intravenous |
| Strength | 1.5mg/vial |
| Market Status | Prescription |
| Company | Scios |
Digital Content 
NEWS #PharmaBuzz
REF. STANDARDS & IMPURITIES
ABOUT THIS PAGE
A Natrecor manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Natrecor, including repackagers and relabelers. The FDA regulates Natrecor manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Natrecor 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 Natrecor supplier is an individual or a company that provides Natrecor active pharmaceutical ingredient (API) or Natrecor finished formulations upon request. The Natrecor suppliers may include Natrecor API manufacturers, exporters, distributors and traders.
click here to find a list of Natrecor suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Natrecor DMF (Drug Master File) is a document detailing the whole manufacturing process of Natrecor active pharmaceutical ingredient (API) in detail. Different forms of Natrecor DMFs exist exist since differing nations have different regulations, such as Natrecor USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Natrecor DMF submitted to regulatory agencies in the US is known as a USDMF. Natrecor USDMF includes data on Natrecor's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Natrecor USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Natrecor suppliers with USDMF on PharmaCompass.
Natrecor 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 Natrecor 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 Natrecor GMP manufacturer or Natrecor GMP API supplier for your needs.
A Natrecor CoA (Certificate of Analysis) is a formal document that attests to Natrecor's compliance with Natrecor specifications and serves as a tool for batch-level quality control.
Natrecor CoA mostly includes findings from lab analyses of a specific batch. For each Natrecor 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.
Natrecor may be tested according to a variety of international standards, such as European Pharmacopoeia (Natrecor EP), Natrecor JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Natrecor USP).
LOOKING FOR A SUPPLIER?
