Synopsis
Synopsis
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CEP/COS
0
JDMF
0
EU WC
0
KDMF
0
NDC API
0
VMF
0
API
0
FDF
0
FDF Dossiers
0
FDA Orange Book
0
Europe
0
Canada
0
Australia
0
South Africa
0
Listed Dossiers
DRUG PRODUCT COMPOSITIONS
0
EDQM
0
USP
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JP
0
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. Archin
2. Casanthranol
3. Emodin
4. Emodin, Frangula
5. Emodin, Rheum
6. Frangula Emodin
7. Frangulic Acid
8. Peristim
9. Rheum Emodin
1. Casanthranol
2. Casanthranol [usan:usp]
3. Casakol
4. 3sj3u7j6v2
5. Hms3264c12
6. Pharmakon1600-01506179
7. Nsc760410
8. Zinc66322924
9. Ccg-213629
10. Nsc 760410
11. Nsc-760410
12. Ab01563152_01
Molecular Weight | 434.4 g/mol |
---|---|
Molecular Formula | C21H22O10 |
XLogP3 | -0.4 |
Hydrogen Bond Donor Count | 7 |
Hydrogen Bond Acceptor Count | 10 |
Rotatable Bond Count | 4 |
Exact Mass | 434.12129689 g/mol |
Monoisotopic Mass | 434.12129689 g/mol |
Topological Polar Surface Area | 177 Ų |
Heavy Atom Count | 31 |
Formal Charge | 0 |
Complexity | 646 |
Isotope Atom Count | 0 |
Defined Atom Stereocenter Count | 6 |
Undefined Atom Stereocenter Count | 0 |
Defined Bond Stereocenter Count | 0 |
Undefined Bond Stereocenter Count | 0 |
Covalently Bonded Unit Count | 1 |
Cathartics
Agents that are used to stimulate evacuation of the bowels. (See all compounds classified as Cathartics.)
Protein Kinase Inhibitors
Agents that inhibit PROTEIN KINASES. (See all compounds classified as Protein Kinase Inhibitors.)
ABOUT THIS PAGE
A Cascara manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cascara, including repackagers and relabelers. The FDA regulates Cascara manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cascara 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 Cascara manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cascara supplier is an individual or a company that provides Cascara active pharmaceutical ingredient (API) or Cascara finished formulations upon request. The Cascara suppliers may include Cascara API manufacturers, exporters, distributors and traders.
click here to find a list of Cascara suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Cascara DMF (Drug Master File) is a document detailing the whole manufacturing process of Cascara active pharmaceutical ingredient (API) in detail. Different forms of Cascara DMFs exist exist since differing nations have different regulations, such as Cascara USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Cascara DMF submitted to regulatory agencies in the US is known as a USDMF. Cascara USDMF includes data on Cascara's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Cascara USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Cascara suppliers with USDMF on PharmaCompass.
Cascara 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 Cascara 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 Cascara GMP manufacturer or Cascara GMP API supplier for your needs.
A Cascara CoA (Certificate of Analysis) is a formal document that attests to Cascara's compliance with Cascara specifications and serves as a tool for batch-level quality control.
Cascara CoA mostly includes findings from lab analyses of a specific batch. For each Cascara 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.
Cascara may be tested according to a variety of international standards, such as European Pharmacopoeia (Cascara EP), Cascara JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Cascara USP).
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