Synopsis
Synopsis
0
CEP/COS
0
JDMF
0
EU WC
0
KDMF
0
NDC API
0
VMF
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
0
News #PharmaBuzz
US Medicaid
NA
Annual Reports
NA
Finished Drug Prices
NA
1. Schembl145070
Molecular Weight | 982.8 g/mol |
---|---|
Molecular Formula | C12H22O35S8 |
XLogP3 | -8.6 |
Hydrogen Bond Donor Count | 8 |
Hydrogen Bond Acceptor Count | 35 |
Rotatable Bond Count | 21 |
Exact Mass | 981.7707318 g/mol |
Monoisotopic Mass | 981.7707318 g/mol |
Topological Polar Surface Area | 604 Ų |
Heavy Atom Count | 55 |
Formal Charge | 0 |
Complexity | 2230 |
Isotope Atom Count | 0 |
Defined Atom Stereocenter Count | 9 |
Undefined Atom Stereocenter Count | 0 |
Defined Bond Stereocenter Count | 0 |
Undefined Bond Stereocenter Count | 0 |
Covalently Bonded Unit Count | 1 |
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 36552
Submission : 2022-02-24
Status : Active
Type : IV
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 11533
Submission : 1995-05-25
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 9475
Submission : 1992-01-02
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 9475
Submission : 1992-01-02
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 36552
Submission : 2022-02-24
Status : Active
Type : IV
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 11533
Submission : 1995-05-25
Status : Inactive
Type : II
About the Company : We provide quality products and services, consistently, reliably responsibly and continuously applying some of the world’s most difficult to handle chemical technologies. Synth...
About the Company : Qfine is a division of Productos Aditivos S.A., the sole European producer of saccharin and cyclamate and a preferred partner to well over 100 companies in the food and pharmaceuti...
About the Company : Established in 2002, Tecoland represents selected cGMP manufacturers with proven capabilities in organic synthesis, fermentation production as well as process and method developmen...
API Imports and Exports
Importing Country | Total Quantity (KGS) |
Average Price (USD/KGS) |
Number of Transactions |
---|
Upgrade, download data, analyse, strategize, subscribe with us
Market Place
Reply
12 Oct 2022
Reply
04 Jul 2022
Reply
23 Feb 2021
Reply
07 May 2020
Reply
30 Mar 2020
Reply
25 Oct 2019
REF. STANDARDS & IMPURITIES
ABOUT THIS PAGE
A Sucrose Octasulfate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sucrose Octasulfate, including repackagers and relabelers. The FDA regulates Sucrose Octasulfate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sucrose Octasulfate 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 Sucrose Octasulfate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Sucrose Octasulfate supplier is an individual or a company that provides Sucrose Octasulfate active pharmaceutical ingredient (API) or Sucrose Octasulfate finished formulations upon request. The Sucrose Octasulfate suppliers may include Sucrose Octasulfate API manufacturers, exporters, distributors and traders.
click here to find a list of Sucrose Octasulfate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Sucrose Octasulfate DMF (Drug Master File) is a document detailing the whole manufacturing process of Sucrose Octasulfate active pharmaceutical ingredient (API) in detail. Different forms of Sucrose Octasulfate DMFs exist exist since differing nations have different regulations, such as Sucrose Octasulfate USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Sucrose Octasulfate DMF submitted to regulatory agencies in the US is known as a USDMF. Sucrose Octasulfate USDMF includes data on Sucrose Octasulfate's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Sucrose Octasulfate USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Sucrose Octasulfate suppliers with USDMF on PharmaCompass.
Sucrose Octasulfate 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 Sucrose Octasulfate 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 Sucrose Octasulfate GMP manufacturer or Sucrose Octasulfate GMP API supplier for your needs.
A Sucrose Octasulfate CoA (Certificate of Analysis) is a formal document that attests to Sucrose Octasulfate's compliance with Sucrose Octasulfate specifications and serves as a tool for batch-level quality control.
Sucrose Octasulfate CoA mostly includes findings from lab analyses of a specific batch. For each Sucrose Octasulfate 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.
Sucrose Octasulfate may be tested according to a variety of international standards, such as European Pharmacopoeia (Sucrose Octasulfate EP), Sucrose Octasulfate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Sucrose Octasulfate USP).
LOOKING FOR A SUPPLIER?