Synopsis
Synopsis
0
API Suppliers
0
USDMF
0
CEP/COS
0
JDMF
0
EU WC
0
KDMF
0
NDC API
0
VMF
0
Listed Suppliers
0
EDQM
0
USP
0
JP
0
Others
0
FDA Orange Book
0
Canada
0
Australia
DRUG PRODUCT COMPOSITIONS
0
US Patents
0
US Exclusivities
0
Health Canada Patents
US Medicaid
NA
Annual Reports
NA
Regulatory FDF Prices
NA
0
FDF
0
Stock Recap #PipelineProspector
0
Weekly News Recap #Phispers
0
News #PharmaBuzz
1. Q26840932
| Molecular Weight | 484.14 g/mol |
|---|---|
| Molecular Formula | Al2H29Mg2O15Si4- |
| Hydrogen Bond Donor Count | 15 |
| Hydrogen Bond Acceptor Count | 15 |
| Rotatable Bond Count | 0 |
| Exact Mass | 482.991512 g/mol |
| Monoisotopic Mass | 482.991512 g/mol |
| Topological Polar Surface Area | 15 Ų |
| Heavy Atom Count | 23 |
| Formal Charge | -1 |
| Complexity | 0 |
| 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 | 23 |
FDF Dossiers
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Europe
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Digital Content
DATA COMPILATION #PharmaFlow
Market Place
ABOUT THIS PAGE
80
PharmaCompass offers a list of Attapulgite 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 Attapulgite manufacturer or Attapulgite supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Attapulgite manufacturer or Attapulgite supplier.
PharmaCompass also assists you with knowing the Attapulgite API Price utilized in the formulation of products. Attapulgite API Price is not always fixed or binding as the Attapulgite Price is obtained through a variety of data sources. The Attapulgite Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Activated attapulgite manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Activated attapulgite, including repackagers and relabelers. The FDA regulates Activated attapulgite manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Activated attapulgite 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 Activated attapulgite supplier is an individual or a company that provides Activated attapulgite active pharmaceutical ingredient (API) or Activated attapulgite finished formulations upon request. The Activated attapulgite suppliers may include Activated attapulgite API manufacturers, exporters, distributors and traders.
Activated attapulgite 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 Activated attapulgite 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 Activated attapulgite GMP manufacturer or Activated attapulgite GMP API supplier for your needs.
A Activated attapulgite CoA (Certificate of Analysis) is a formal document that attests to Activated attapulgite's compliance with Activated attapulgite specifications and serves as a tool for batch-level quality control.
Activated attapulgite CoA mostly includes findings from lab analyses of a specific batch. For each Activated attapulgite 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.
Activated attapulgite may be tested according to a variety of international standards, such as European Pharmacopoeia (Activated attapulgite EP), Activated attapulgite JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Activated attapulgite USP).
