Synopsis
Synopsis
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
US Medicaid
NA
Annual Reports
NA
Finished Drug Prices
NA
1. Akos024437838
| Molecular Weight | 311.29 g/mol |
|---|---|
| Molecular Formula | C11H21NO9 |
| Hydrogen Bond Donor Count | 5 |
| Hydrogen Bond Acceptor Count | 9 |
| Rotatable Bond Count | 6 |
| Exact Mass | 311.12163125 g/mol |
| Monoisotopic Mass | 311.12163125 g/mol |
| Topological Polar Surface Area | 175 Ų |
| Heavy Atom Count | 21 |
| Formal Charge | 0 |
| Complexity | 267 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 3 |
| 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]
USDMF
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 
Digital Content
NEWS #PharmaBuzz
Market Place
ABOUT THIS PAGE
A L-Carnitine Tartrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of L-Carnitine Tartrate, including repackagers and relabelers. The FDA regulates L-Carnitine Tartrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. L-Carnitine Tartrate 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 L-Carnitine Tartrate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A L-Carnitine Tartrate supplier is an individual or a company that provides L-Carnitine Tartrate active pharmaceutical ingredient (API) or L-Carnitine Tartrate finished formulations upon request. The L-Carnitine Tartrate suppliers may include L-Carnitine Tartrate API manufacturers, exporters, distributors and traders.
click here to find a list of L-Carnitine Tartrate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A L-Carnitine Tartrate DMF (Drug Master File) is a document detailing the whole manufacturing process of L-Carnitine Tartrate active pharmaceutical ingredient (API) in detail. Different forms of L-Carnitine Tartrate DMFs exist exist since differing nations have different regulations, such as L-Carnitine Tartrate USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A L-Carnitine Tartrate DMF submitted to regulatory agencies in the US is known as a USDMF. L-Carnitine Tartrate USDMF includes data on L-Carnitine Tartrate's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The L-Carnitine Tartrate USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of L-Carnitine Tartrate suppliers with USDMF on PharmaCompass.
L-Carnitine Tartrate 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 L-Carnitine Tartrate 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 L-Carnitine Tartrate GMP manufacturer or L-Carnitine Tartrate GMP API supplier for your needs.
A L-Carnitine Tartrate CoA (Certificate of Analysis) is a formal document that attests to L-Carnitine Tartrate's compliance with L-Carnitine Tartrate specifications and serves as a tool for batch-level quality control.
L-Carnitine Tartrate CoA mostly includes findings from lab analyses of a specific batch. For each L-Carnitine Tartrate 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.
L-Carnitine Tartrate may be tested according to a variety of international standards, such as European Pharmacopoeia (L-Carnitine Tartrate EP), L-Carnitine Tartrate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (L-Carnitine Tartrate USP).
LOOKING FOR A SUPPLIER?
