Synopsis
Synopsis
0
CEP/COS
0
JDMF
0
EU WC
0
KDMF
0
NDC API
0
VMF
0
API
0
FDF
0
FDA Orange Book
0
Europe
0
Canada
0
Australia
0
Listed Dossiers
DRUG PRODUCT COMPOSITIONS
0
US Patents
0
US Exclusivities
0
Health Canada Patents
0
Data Compilation #PharmaFlow
0
Stock Recap #PipelineProspector
0
Weekly News Recap #Phispers
US Medicaid
NA
Annual Reports
NA
Finished Drug Prices
NA
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 |
API SUPPLIERS
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]
Digital Content
NEWS #PharmaBuzz
REF. STANDARDS & IMPURITIES
ABOUT THIS PAGE
A Human Epidermal Growth Factor manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Human Epidermal Growth Factor, including repackagers and relabelers. The FDA regulates Human Epidermal Growth Factor manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Human Epidermal Growth Factor 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 Human Epidermal Growth Factor manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Human Epidermal Growth Factor supplier is an individual or a company that provides Human Epidermal Growth Factor active pharmaceutical ingredient (API) or Human Epidermal Growth Factor finished formulations upon request. The Human Epidermal Growth Factor suppliers may include Human Epidermal Growth Factor API manufacturers, exporters, distributors and traders.
click here to find a list of Human Epidermal Growth Factor suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Human Epidermal Growth Factor DMF (Drug Master File) is a document detailing the whole manufacturing process of Human Epidermal Growth Factor active pharmaceutical ingredient (API) in detail. Different forms of Human Epidermal Growth Factor DMFs exist exist since differing nations have different regulations, such as Human Epidermal Growth Factor USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Human Epidermal Growth Factor DMF submitted to regulatory agencies in the US is known as a USDMF. Human Epidermal Growth Factor USDMF includes data on Human Epidermal Growth Factor's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Human Epidermal Growth Factor USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Human Epidermal Growth Factor suppliers with USDMF on PharmaCompass.
Human Epidermal Growth Factor 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 Human Epidermal Growth Factor 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 Human Epidermal Growth Factor GMP manufacturer or Human Epidermal Growth Factor GMP API supplier for your needs.
A Human Epidermal Growth Factor CoA (Certificate of Analysis) is a formal document that attests to Human Epidermal Growth Factor's compliance with Human Epidermal Growth Factor specifications and serves as a tool for batch-level quality control.
Human Epidermal Growth Factor CoA mostly includes findings from lab analyses of a specific batch. For each Human Epidermal Growth Factor 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.
Human Epidermal Growth Factor may be tested according to a variety of international standards, such as European Pharmacopoeia (Human Epidermal Growth Factor EP), Human Epidermal Growth Factor JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Human Epidermal Growth Factor USP).
LOOKING FOR A SUPPLIER?
