Synopsis
Synopsis
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CEP/COS
0
JDMF
0
EU WC
0
KDMF
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NDC API
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VMF
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Listed Suppliers
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FDF Dossiers
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FDA Orange Book
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Europe
0
Canada
0
Australia
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South Africa
0
Listed Dossiers
DRUG PRODUCT COMPOSITIONS
0
US Patents
0
US Exclusivities
0
Health Canada Patents
US Medicaid
NA
Annual Reports
NA
Regulatory FDF Prices
NA
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API
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FDF
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Data Compilation #PharmaFlow
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Stock Recap #PipelineProspector
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Weekly News Recap #Phispers
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News #PharmaBuzz
Molecular Weight | 596.7 g/mol |
---|---|
Molecular Formula | C29H36N6O6S |
XLogP3 | -2.1 |
Hydrogen Bond Donor Count | 7 |
Hydrogen Bond Acceptor Count | 8 |
Rotatable Bond Count | 16 |
Exact Mass | 596.24170406 g/mol |
Monoisotopic Mass | 596.24170406 g/mol |
Topological Polar Surface Area | 235 Ų |
Heavy Atom Count | 42 |
Formal Charge | 0 |
Complexity | 948 |
Isotope Atom Count | 0 |
Defined Atom Stereocenter Count | 3 |
Undefined Atom Stereocenter Count | 1 |
Defined Bond Stereocenter Count | 0 |
Undefined Bond Stereocenter Count | 0 |
Covalently Bonded Unit Count | 1 |
REF. STANDARDS & IMPURITIES
ABOUT THIS PAGE
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PharmaCompass offers a list of Tetragastrin 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 Tetragastrin manufacturer or Tetragastrin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Tetragastrin manufacturer or Tetragastrin supplier.
PharmaCompass also assists you with knowing the Tetragastrin API Price utilized in the formulation of products. Tetragastrin API Price is not always fixed or binding as the Tetragastrin Price is obtained through a variety of data sources. The Tetragastrin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Tetragastrin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tetragastrin, including repackagers and relabelers. The FDA regulates Tetragastrin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tetragastrin 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 Tetragastrin supplier is an individual or a company that provides Tetragastrin active pharmaceutical ingredient (API) or Tetragastrin finished formulations upon request. The Tetragastrin suppliers may include Tetragastrin API manufacturers, exporters, distributors and traders.
click here to find a list of Tetragastrin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Tetragastrin DMF (Drug Master File) is a document detailing the whole manufacturing process of Tetragastrin active pharmaceutical ingredient (API) in detail. Different forms of Tetragastrin DMFs exist exist since differing nations have different regulations, such as Tetragastrin USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Tetragastrin DMF submitted to regulatory agencies in the US is known as a USDMF. Tetragastrin USDMF includes data on Tetragastrin's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Tetragastrin USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Tetragastrin suppliers with USDMF on PharmaCompass.
Tetragastrin 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 Tetragastrin 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 Tetragastrin GMP manufacturer or Tetragastrin GMP API supplier for your needs.
A Tetragastrin CoA (Certificate of Analysis) is a formal document that attests to Tetragastrin's compliance with Tetragastrin specifications and serves as a tool for batch-level quality control.
Tetragastrin CoA mostly includes findings from lab analyses of a specific batch. For each Tetragastrin 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.
Tetragastrin may be tested according to a variety of international standards, such as European Pharmacopoeia (Tetragastrin EP), Tetragastrin JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Tetragastrin USP).