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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FDA Orange Book
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Europe
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Canada
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Australia
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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
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API
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Data Compilation #PharmaFlow
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1. Beta Urogastrone
2. Beta-urogastrone
3. Egf
4. Epidermal Growth Factor-urogastrone
5. Growth Factor, Epidermal
6. Growth Factor-urogastrone, Epidermal
7. Human Urinary Gastric Inhibitor
8. Urogastrone
1. 62229-50-9
2. Gastrone, Uro-
3. Uroanthelone
4. Uroenterone
5. Urogastron
6. Urogastrone
7. Kutrol
8. Beta-urogastrone
9. Anthelone U
10. Urogastrone [jan]
11. Gastrone, Gamma-uro-
12. Gastrone, Beta-uro- (human)
13. Epidermal Growth Factor (egf)
14. Ccris 7234
15. Einecs 263-468-7
16. Epidermal Growth Factor-urogastrone
Molecular Weight | 6046 g/mol |
---|---|
Molecular Formula | C257H381N73O83S7 |
XLogP3 | -19.6 |
Hydrogen Bond Donor Count | 96 |
Hydrogen Bond Acceptor Count | 96 |
Rotatable Bond Count | 193 |
Exact Mass | 6043.5948607 g/mol |
Monoisotopic Mass | 6041.5881511 g/mol |
Topological Polar Surface Area | 2560 Ų |
Heavy Atom Count | 420 |
Formal Charge | 0 |
Complexity | 15400 |
Isotope Atom Count | 0 |
Defined Atom Stereocenter Count | 51 |
Undefined Atom Stereocenter Count | 0 |
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 Epidermal Growth Factor 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 Epidermal Growth Factor manufacturer or Epidermal Growth Factor supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Epidermal Growth Factor manufacturer or Epidermal Growth Factor supplier.
PharmaCompass also assists you with knowing the Epidermal Growth Factor API Price utilized in the formulation of products. Epidermal Growth Factor API Price is not always fixed or binding as the Epidermal Growth Factor Price is obtained through a variety of data sources. The Epidermal Growth Factor Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A EGF manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of EGF, including repackagers and relabelers. The FDA regulates EGF manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. EGF 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 EGF manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A EGF supplier is an individual or a company that provides EGF active pharmaceutical ingredient (API) or EGF finished formulations upon request. The EGF suppliers may include EGF API manufacturers, exporters, distributors and traders.
click here to find a list of EGF suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A EGF DMF (Drug Master File) is a document detailing the whole manufacturing process of EGF active pharmaceutical ingredient (API) in detail. Different forms of EGF DMFs exist exist since differing nations have different regulations, such as EGF USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A EGF DMF submitted to regulatory agencies in the US is known as a USDMF. EGF USDMF includes data on EGF's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The EGF USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of EGF suppliers with USDMF on PharmaCompass.
EGF 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 EGF 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 EGF GMP manufacturer or EGF GMP API supplier for your needs.
A EGF CoA (Certificate of Analysis) is a formal document that attests to EGF's compliance with EGF specifications and serves as a tool for batch-level quality control.
EGF CoA mostly includes findings from lab analyses of a specific batch. For each EGF 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.
EGF may be tested according to a variety of international standards, such as European Pharmacopoeia (EGF EP), EGF JP (Japanese Pharmacopeia) and the US Pharmacopoeia (EGF USP).