Synopsis
Synopsis
0
USDMF
0
CEP/COS
0
JDMF
0
EU WC
0
KDMF
0
NDC API
0
VMF
0
FDF
0
FDA Orange Book
0
Europe
0
Canada
0
Australia
0
South Africa
DRUG PRODUCT COMPOSITIONS
0
EDQM
0
USP
0
JP
0
Others
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. Chromium Dinicotinate
2. Chromium Polynicotinate
1. Chromium Polynicotinate
2. 64452-96-6
3. Chromium;pyridine-3-carboxylate
| Molecular Weight | 174.10 g/mol |
|---|---|
| Molecular Formula | C6H4CrNO2- |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 0 |
| Exact Mass | 173.964708 g/mol |
| Monoisotopic Mass | 173.964708 g/mol |
| Topological Polar Surface Area | 53 Ų |
| Heavy Atom Count | 10 |
| Formal Charge | -1 |
| Complexity | 108 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 2 |
API SUPPLIERS
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]
Listed Suppliers
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]API Reference Price
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
ABOUT THIS PAGE
A Chromium Polynicotinate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Chromium Polynicotinate, including repackagers and relabelers. The FDA regulates Chromium Polynicotinate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Chromium Polynicotinate 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 Chromium Polynicotinate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Chromium Polynicotinate supplier is an individual or a company that provides Chromium Polynicotinate active pharmaceutical ingredient (API) or Chromium Polynicotinate finished formulations upon request. The Chromium Polynicotinate suppliers may include Chromium Polynicotinate API manufacturers, exporters, distributors and traders.
click here to find a list of Chromium Polynicotinate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
Chromium Polynicotinate 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 Chromium Polynicotinate 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 Chromium Polynicotinate GMP manufacturer or Chromium Polynicotinate GMP API supplier for your needs.
A Chromium Polynicotinate CoA (Certificate of Analysis) is a formal document that attests to Chromium Polynicotinate's compliance with Chromium Polynicotinate specifications and serves as a tool for batch-level quality control.
Chromium Polynicotinate CoA mostly includes findings from lab analyses of a specific batch. For each Chromium Polynicotinate 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.
Chromium Polynicotinate may be tested according to a variety of international standards, such as European Pharmacopoeia (Chromium Polynicotinate EP), Chromium Polynicotinate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Chromium Polynicotinate USP).
LOOKING FOR A SUPPLIER?
