Synopsis
Synopsis
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CEP/COS
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JDMF
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EU WC
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KDMF
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NDC API
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VMF
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Listed Suppliers
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API
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FDF
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FDF Dossiers
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FDA Orange Book
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Europe
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Canada
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Australia
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South Africa
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Listed Dossiers
DRUG PRODUCT COMPOSITIONS
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EDQM
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USP
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JP
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Others
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US Patents
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US Exclusivities
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Health Canada Patents
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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
US Medicaid
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Annual Reports
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Finished Drug Prices
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1. Schembl714208
Molecular Weight | 523.1 g/mol |
---|---|
Molecular Formula | C24H50MgO6S2 |
Hydrogen Bond Donor Count | 0 |
Hydrogen Bond Acceptor Count | 6 |
Rotatable Bond Count | 20 |
Exact Mass | 522.2899233 g/mol |
Monoisotopic Mass | 522.2899233 g/mol |
Topological Polar Surface Area | 131 Ų |
Heavy Atom Count | 33 |
Formal Charge | 0 |
Complexity | 216 |
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 | 3 |
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 2059
Submission : 1973-01-12
Status : Inactive
Type : II
API Imports and Exports
Importing Country | Total Quantity (KGS) |
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ABOUT THIS PAGE
A Dodecyl Sulfate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dodecyl Sulfate, including repackagers and relabelers. The FDA regulates Dodecyl Sulfate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dodecyl Sulfate 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 Dodecyl Sulfate supplier is an individual or a company that provides Dodecyl Sulfate active pharmaceutical ingredient (API) or Dodecyl Sulfate finished formulations upon request. The Dodecyl Sulfate suppliers may include Dodecyl Sulfate API manufacturers, exporters, distributors and traders.
click here to find a list of Dodecyl Sulfate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Dodecyl Sulfate DMF (Drug Master File) is a document detailing the whole manufacturing process of Dodecyl Sulfate active pharmaceutical ingredient (API) in detail. Different forms of Dodecyl Sulfate DMFs exist exist since differing nations have different regulations, such as Dodecyl Sulfate USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Dodecyl Sulfate DMF submitted to regulatory agencies in the US is known as a USDMF. Dodecyl Sulfate USDMF includes data on Dodecyl Sulfate's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Dodecyl Sulfate USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Dodecyl Sulfate suppliers with USDMF on PharmaCompass.
Dodecyl Sulfate 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 Dodecyl Sulfate 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 Dodecyl Sulfate GMP manufacturer or Dodecyl Sulfate GMP API supplier for your needs.
A Dodecyl Sulfate CoA (Certificate of Analysis) is a formal document that attests to Dodecyl Sulfate's compliance with Dodecyl Sulfate specifications and serves as a tool for batch-level quality control.
Dodecyl Sulfate CoA mostly includes findings from lab analyses of a specific batch. For each Dodecyl Sulfate 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.
Dodecyl Sulfate may be tested according to a variety of international standards, such as European Pharmacopoeia (Dodecyl Sulfate EP), Dodecyl Sulfate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Dodecyl Sulfate USP).
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