Synopsis
Synopsis
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USDMF
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CEP/COS
0
JDMF
0
EU WC
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KDMF
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NDC API
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VMF
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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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US Patents
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US Exclusivities
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Health Canada Patents
US Medicaid
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Annual Reports
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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 | 922.9 g/mol |
---|---|
Molecular Formula | C46H50O20 |
Hydrogen Bond Donor Count | 12 |
Hydrogen Bond Acceptor Count | 20 |
Rotatable Bond Count | 6 |
Exact Mass | 922.28954398 g/mol |
Monoisotopic Mass | 922.28954398 g/mol |
Topological Polar Surface Area | 332 Ų |
Heavy Atom Count | 66 |
Formal Charge | 0 |
Complexity | 1170 |
Isotope Atom Count | 0 |
Defined Atom Stereocenter Count | 9 |
Undefined Atom Stereocenter Count | 1 |
Defined Bond Stereocenter Count | 1 |
Undefined Bond Stereocenter Count | 0 |
Covalently Bonded Unit Count | 4 |
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API Imports and Exports
Importing Country | Total Quantity (KGS) |
Average Price (USD/KGS) |
Number of Transactions |
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PharmaCompass offers a list of Aniseed 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 Aniseed manufacturer or Aniseed supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Aniseed manufacturer or Aniseed supplier.
PharmaCompass also assists you with knowing the Aniseed API Price utilized in the formulation of products. Aniseed API Price is not always fixed or binding as the Aniseed Price is obtained through a variety of data sources. The Aniseed Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Anise (Pimpinella anisum L.) manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Anise (Pimpinella anisum L.), including repackagers and relabelers. The FDA regulates Anise (Pimpinella anisum L.) manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Anise (Pimpinella anisum L.) 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 Anise (Pimpinella anisum L.) manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Anise (Pimpinella anisum L.) supplier is an individual or a company that provides Anise (Pimpinella anisum L.) active pharmaceutical ingredient (API) or Anise (Pimpinella anisum L.) finished formulations upon request. The Anise (Pimpinella anisum L.) suppliers may include Anise (Pimpinella anisum L.) API manufacturers, exporters, distributors and traders.
click here to find a list of Anise (Pimpinella anisum L.) suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
Anise (Pimpinella anisum L.) 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 Anise (Pimpinella anisum L.) 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 Anise (Pimpinella anisum L.) GMP manufacturer or Anise (Pimpinella anisum L.) GMP API supplier for your needs.
A Anise (Pimpinella anisum L.) CoA (Certificate of Analysis) is a formal document that attests to Anise (Pimpinella anisum L.)'s compliance with Anise (Pimpinella anisum L.) specifications and serves as a tool for batch-level quality control.
Anise (Pimpinella anisum L.) CoA mostly includes findings from lab analyses of a specific batch. For each Anise (Pimpinella anisum L.) 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.
Anise (Pimpinella anisum L.) may be tested according to a variety of international standards, such as European Pharmacopoeia (Anise (Pimpinella anisum L.) EP), Anise (Pimpinella anisum L.) JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Anise (Pimpinella anisum L.) USP).