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1. 4-(1-hydroxy-2-(methylamino)ethyl)-1,2-benzenediol
2. Acetate, Epinephrine
3. Adrenaline
4. Adrenaline Acid Tartrate
5. Adrenaline Bitartrate
6. Adrenaline Hydrochloride
7. Epifrin
8. Epinephrine
9. Epinephrine Acetate
10. Epinephrine Bitartrate
11. Epinephrine Hydrochloride
12. Epitrate
13. Lyophrin
14. Medihaler-epi
1. (-)-epinephrine Bitartrate
2. Adrenaline Bitartrate
3. Mls000028381
4. Epinephrine D-bitartrate
5. L-epinephrine Bitartrate
6. Smr000058630
7. Adrenaline Bitartate
8. Adrenaline (as Tartrate)
9. Sr-01000075267
10. L-epinephrine Hydrogen Tartrate
11. Adrenalin Tartrate
12. Nsc-756755
13. Opera_id_1462
14. Epinephrini Hydrogenotartras
15. Lopac0_000502
16. Schembl597216
17. Chembl1256958
18. L-adrenaline Hydrogen Bitartrate
19. L-epinephrine Hydrogen Bitartrate
20. Hms2233k16
21. Hms3261f05
22. Tox21_500502
23. Akos030504417
24. Ccg-221806
25. Lp00502
26. Ncgc00093902-01
27. Ncgc00261187-01
28. A0175
29. Eu-0100502
30. E 4375
31. Sr-01000075267-1
32. Sr-01000075267-4
33. Sr-01000075267-6
Molecular Weight | 333.29 g/mol |
---|---|
Molecular Formula | C13H19NO9 |
Hydrogen Bond Donor Count | 8 |
Hydrogen Bond Acceptor Count | 10 |
Rotatable Bond Count | 6 |
Exact Mass | 333.10598118 g/mol |
Monoisotopic Mass | 333.10598118 g/mol |
Topological Polar Surface Area | 188 Ų |
Heavy Atom Count | 23 |
Formal Charge | 0 |
Complexity | 288 |
Isotope Atom Count | 0 |
Defined Atom Stereocenter Count | 1 |
Undefined Atom Stereocenter Count | 2 |
Defined Bond Stereocenter Count | 0 |
Undefined Bond Stereocenter Count | 0 |
Covalently Bonded Unit Count | 2 |
Adrenergic alpha-Agonists
Drugs that selectively bind to and activate alpha adrenergic receptors. (See all compounds classified as Adrenergic alpha-Agonists.)
Adrenergic beta-Agonists
Drugs that selectively bind to and activate beta-adrenergic receptors. (See all compounds classified as Adrenergic beta-Agonists.)
Bronchodilator Agents
Agents that cause an increase in the expansion of a bronchus or bronchial tubes. (See all compounds classified as Bronchodilator Agents.)
Mydriatics
Agents that dilate the pupil. They may be either sympathomimetics or parasympatholytics. (See all compounds classified as Mydriatics.)
Sympathomimetics
Drugs that mimic the effects of stimulating postganglionic adrenergic sympathetic nerves. Included here are drugs that directly stimulate adrenergic receptors and drugs that act indirectly by provoking the release of adrenergic transmitters. (See all compounds classified as Sympathomimetics.)
Vasoconstrictor Agents
Drugs used to cause constriction of the blood vessels. (See all compounds classified as Vasoconstrictor Agents.)
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PharmaCompass offers a list of Epinephrine Bitartrate 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 Epinephrine Bitartrate manufacturer or Epinephrine Bitartrate supplier for your needs.
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A Epinephrine bitartrate, Adrenalinium, D02149, Adrenalinetartrate, Adrenaline tatrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Epinephrine bitartrate, Adrenalinium, D02149, Adrenalinetartrate, Adrenaline tatrate, including repackagers and relabelers. The FDA regulates Epinephrine bitartrate, Adrenalinium, D02149, Adrenalinetartrate, Adrenaline tatrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Epinephrine bitartrate, Adrenalinium, D02149, Adrenalinetartrate, Adrenaline tatrate API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Epinephrine bitartrate, Adrenalinium, D02149, Adrenalinetartrate, Adrenaline tatrate supplier is an individual or a company that provides Epinephrine bitartrate, Adrenalinium, D02149, Adrenalinetartrate, Adrenaline tatrate active pharmaceutical ingredient (API) or Epinephrine bitartrate, Adrenalinium, D02149, Adrenalinetartrate, Adrenaline tatrate finished formulations upon request. The Epinephrine bitartrate, Adrenalinium, D02149, Adrenalinetartrate, Adrenaline tatrate suppliers may include Epinephrine bitartrate, Adrenalinium, D02149, Adrenalinetartrate, Adrenaline tatrate API manufacturers, exporters, distributors and traders.
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A Epinephrine bitartrate, Adrenalinium, D02149, Adrenalinetartrate, Adrenaline tatrate DMF (Drug Master File) is a document detailing the whole manufacturing process of Epinephrine bitartrate, Adrenalinium, D02149, Adrenalinetartrate, Adrenaline tatrate active pharmaceutical ingredient (API) in detail. Different forms of Epinephrine bitartrate, Adrenalinium, D02149, Adrenalinetartrate, Adrenaline tatrate DMFs exist exist since differing nations have different regulations, such as Epinephrine bitartrate, Adrenalinium, D02149, Adrenalinetartrate, Adrenaline tatrate USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Epinephrine bitartrate, Adrenalinium, D02149, Adrenalinetartrate, Adrenaline tatrate DMF submitted to regulatory agencies in the US is known as a USDMF. Epinephrine bitartrate, Adrenalinium, D02149, Adrenalinetartrate, Adrenaline tatrate USDMF includes data on Epinephrine bitartrate, Adrenalinium, D02149, Adrenalinetartrate, Adrenaline tatrate's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Epinephrine bitartrate, Adrenalinium, D02149, Adrenalinetartrate, Adrenaline tatrate USDMF is kept confidential to protect the manufacturer’s intellectual property.
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The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The Epinephrine bitartrate, Adrenalinium, D02149, Adrenalinetartrate, Adrenaline tatrate Drug Master File in Japan (Epinephrine bitartrate, Adrenalinium, D02149, Adrenalinetartrate, Adrenaline tatrate JDMF) empowers Epinephrine bitartrate, Adrenalinium, D02149, Adrenalinetartrate, Adrenaline tatrate API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the Epinephrine bitartrate, Adrenalinium, D02149, Adrenalinetartrate, Adrenaline tatrate JDMF during the approval evaluation for pharmaceutical products. At the time of Epinephrine bitartrate, Adrenalinium, D02149, Adrenalinetartrate, Adrenaline tatrate JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a Epinephrine bitartrate, Adrenalinium, D02149, Adrenalinetartrate, Adrenaline tatrate Drug Master File in Korea (Epinephrine bitartrate, Adrenalinium, D02149, Adrenalinetartrate, Adrenaline tatrate KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Epinephrine bitartrate, Adrenalinium, D02149, Adrenalinetartrate, Adrenaline tatrate. The MFDS reviews the Epinephrine bitartrate, Adrenalinium, D02149, Adrenalinetartrate, Adrenaline tatrate KDMF as part of the drug registration process and uses the information provided in the Epinephrine bitartrate, Adrenalinium, D02149, Adrenalinetartrate, Adrenaline tatrate KDMF to evaluate the safety and efficacy of the drug.
After submitting a Epinephrine bitartrate, Adrenalinium, D02149, Adrenalinetartrate, Adrenaline tatrate KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their Epinephrine bitartrate, Adrenalinium, D02149, Adrenalinetartrate, Adrenaline tatrate API can apply through the Korea Drug Master File (KDMF).
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A Epinephrine bitartrate, Adrenalinium, D02149, Adrenalinetartrate, Adrenaline tatrate CEP of the European Pharmacopoeia monograph is often referred to as a Epinephrine bitartrate, Adrenalinium, D02149, Adrenalinetartrate, Adrenaline tatrate Certificate of Suitability (COS). The purpose of a Epinephrine bitartrate, Adrenalinium, D02149, Adrenalinetartrate, Adrenaline tatrate CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Epinephrine bitartrate, Adrenalinium, D02149, Adrenalinetartrate, Adrenaline tatrate EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Epinephrine bitartrate, Adrenalinium, D02149, Adrenalinetartrate, Adrenaline tatrate to their clients by showing that a Epinephrine bitartrate, Adrenalinium, D02149, Adrenalinetartrate, Adrenaline tatrate CEP has been issued for it. The manufacturer submits a Epinephrine bitartrate, Adrenalinium, D02149, Adrenalinetartrate, Adrenaline tatrate CEP (COS) as part of the market authorization procedure, and it takes on the role of a Epinephrine bitartrate, Adrenalinium, D02149, Adrenalinetartrate, Adrenaline tatrate CEP holder for the record. Additionally, the data presented in the Epinephrine bitartrate, Adrenalinium, D02149, Adrenalinetartrate, Adrenaline tatrate CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Epinephrine bitartrate, Adrenalinium, D02149, Adrenalinetartrate, Adrenaline tatrate DMF.
A Epinephrine bitartrate, Adrenalinium, D02149, Adrenalinetartrate, Adrenaline tatrate CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Epinephrine bitartrate, Adrenalinium, D02149, Adrenalinetartrate, Adrenaline tatrate CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
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A Epinephrine bitartrate, Adrenalinium, D02149, Adrenalinetartrate, Adrenaline tatrate written confirmation (Epinephrine bitartrate, Adrenalinium, D02149, Adrenalinetartrate, Adrenaline tatrate WC) is an official document issued by a regulatory agency to a Epinephrine bitartrate, Adrenalinium, D02149, Adrenalinetartrate, Adrenaline tatrate manufacturer, verifying that the manufacturing facility of a Epinephrine bitartrate, Adrenalinium, D02149, Adrenalinetartrate, Adrenaline tatrate active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Epinephrine bitartrate, Adrenalinium, D02149, Adrenalinetartrate, Adrenaline tatrate APIs or Epinephrine bitartrate, Adrenalinium, D02149, Adrenalinetartrate, Adrenaline tatrate finished pharmaceutical products to another nation, regulatory agencies frequently require a Epinephrine bitartrate, Adrenalinium, D02149, Adrenalinetartrate, Adrenaline tatrate WC (written confirmation) as part of the regulatory process.
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National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing Epinephrine bitartrate, Adrenalinium, D02149, Adrenalinetartrate, Adrenaline tatrate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Epinephrine bitartrate, Adrenalinium, D02149, Adrenalinetartrate, Adrenaline tatrate API and other APIs are published in this directory by the FDA.
The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.
Pharmaceutical companies that manufacture Epinephrine bitartrate, Adrenalinium, D02149, Adrenalinetartrate, Adrenaline tatrate as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.
The NDC directory also contains data on finished compounded human drug products that contain Epinephrine bitartrate, Adrenalinium, D02149, Adrenalinetartrate, Adrenaline tatrate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Epinephrine bitartrate, Adrenalinium, D02149, Adrenalinetartrate, Adrenaline tatrate NDC to their finished compounded human drug products, they may choose to do so.
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Epinephrine bitartrate, Adrenalinium, D02149, Adrenalinetartrate, Adrenaline tatrate 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 Epinephrine bitartrate, Adrenalinium, D02149, Adrenalinetartrate, Adrenaline tatrate 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 Epinephrine bitartrate, Adrenalinium, D02149, Adrenalinetartrate, Adrenaline tatrate GMP manufacturer or Epinephrine bitartrate, Adrenalinium, D02149, Adrenalinetartrate, Adrenaline tatrate GMP API supplier for your needs.
A Epinephrine bitartrate, Adrenalinium, D02149, Adrenalinetartrate, Adrenaline tatrate CoA (Certificate of Analysis) is a formal document that attests to Epinephrine bitartrate, Adrenalinium, D02149, Adrenalinetartrate, Adrenaline tatrate's compliance with Epinephrine bitartrate, Adrenalinium, D02149, Adrenalinetartrate, Adrenaline tatrate specifications and serves as a tool for batch-level quality control.
Epinephrine bitartrate, Adrenalinium, D02149, Adrenalinetartrate, Adrenaline tatrate CoA mostly includes findings from lab analyses of a specific batch. For each Epinephrine bitartrate, Adrenalinium, D02149, Adrenalinetartrate, Adrenaline tatrate 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.
Epinephrine bitartrate, Adrenalinium, D02149, Adrenalinetartrate, Adrenaline tatrate may be tested according to a variety of international standards, such as European Pharmacopoeia (Epinephrine bitartrate, Adrenalinium, D02149, Adrenalinetartrate, Adrenaline tatrate EP), Epinephrine bitartrate, Adrenalinium, D02149, Adrenalinetartrate, Adrenaline tatrate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Epinephrine bitartrate, Adrenalinium, D02149, Adrenalinetartrate, Adrenaline tatrate USP).