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DRUG PRODUCT COMPOSITIONS0
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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.)
API SUPPLIERS
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USDMF
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| Importing Country | Total Quantity (KGS) |
Average Price (USD/KGS) |
Number of Transactions |
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Drugs in Development
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DOSAGE - INJECTABLE;INJECTION - 0.25%
USFDA APPLICATION NUMBER - 16964
DOSAGE - INJECTABLE;INJECTION - 0.25%;0.0091M...DOSAGE - INJECTABLE;INJECTION - 0.25%;0.0091MG/ML
USFDA APPLICATION NUMBER - 16964
DOSAGE - INJECTABLE;INJECTION - 0.5%
USFDA APPLICATION NUMBER - 16964
DOSAGE - INJECTABLE;INJECTION - 0.5%;0.0091MG...DOSAGE - INJECTABLE;INJECTION - 0.5%;0.0091MG/ML
USFDA APPLICATION NUMBER - 16964
DOSAGE - INJECTABLE;INJECTION - 0.75%
USFDA APPLICATION NUMBER - 16964
DOSAGE - INJECTABLE;INJECTION - 0.75%;0.0091M...DOSAGE - INJECTABLE;INJECTION - 0.75%;0.0091MG/ML
USFDA APPLICATION NUMBER - 16964
DOSAGE - INJECTABLE;INJECTION - 0.25%
USFDA APPLICATION NUMBER - 18304
DOSAGE - INJECTABLE;INJECTION - 0.5%
USFDA APPLICATION NUMBER - 18304
DOSAGE - INJECTABLE;INJECTION - 0.5%;0.0091MG...DOSAGE - INJECTABLE;INJECTION - 0.5%;0.0091MG/ML
USFDA APPLICATION NUMBER - 18304
DOSAGE - INJECTABLE;INJECTION - 0.75%
USFDA APPLICATION NUMBER - 18304
DOSAGE - INJECTABLE;INJECTION - 0.75%;0.0091M...DOSAGE - INJECTABLE;INJECTION - 0.75%;0.0091MG/ML
USFDA APPLICATION NUMBER - 18304
DOSAGE - INJECTABLE;INJECTION - 4%; EQ 0.0085...DOSAGE - INJECTABLE;INJECTION - 4%; EQ 0.0085MG BASE/1.7ML (4%; EQ 0.005MG BASE/ML)
USFDA APPLICATION NUMBER - 20971
DOSAGE - INJECTABLE;INJECTION - 4%;EQ 0.017MG...DOSAGE - INJECTABLE;INJECTION - 4%;EQ 0.017MG BASE/1.7ML (4%;EQ 0.01MG BASE/ML)
USFDA APPLICATION NUMBER - 20971
DOSAGE - INJECTABLE;INJECTION - 0.5%;0.0091MG...DOSAGE - INJECTABLE;INJECTION - 0.5%;0.0091MG/ML
USFDA APPLICATION NUMBER - 22046
DOSAGE - INJECTABLE;INJECTION - EQ 0.02MG BAS...DOSAGE - INJECTABLE;INJECTION - EQ 0.02MG BASE/ML;2%
USFDA APPLICATION NUMBER - 88389
DOSAGE - INJECTABLE;INJECTION - EQ 0.01MG BAS...DOSAGE - INJECTABLE;INJECTION - EQ 0.01MG BASE/ML;2%
USFDA APPLICATION NUMBER - 88390
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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.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Epinephrine Bitartrate manufacturer or Epinephrine Bitartrate supplier.
PharmaCompass also assists you with knowing the Epinephrine Bitartrate API Price utilized in the formulation of products. Epinephrine Bitartrate API Price is not always fixed or binding as the Epinephrine Bitartrate Price is obtained through a variety of data sources. The Epinephrine Bitartrate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A LIGNOSPAN STANDARD manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of LIGNOSPAN STANDARD, including repackagers and relabelers. The FDA regulates LIGNOSPAN STANDARD manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. LIGNOSPAN STANDARD 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 LIGNOSPAN STANDARD manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A LIGNOSPAN STANDARD supplier is an individual or a company that provides LIGNOSPAN STANDARD active pharmaceutical ingredient (API) or LIGNOSPAN STANDARD finished formulations upon request. The LIGNOSPAN STANDARD suppliers may include LIGNOSPAN STANDARD API manufacturers, exporters, distributors and traders.
click here to find a list of LIGNOSPAN STANDARD suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A LIGNOSPAN STANDARD DMF (Drug Master File) is a document detailing the whole manufacturing process of LIGNOSPAN STANDARD active pharmaceutical ingredient (API) in detail. Different forms of LIGNOSPAN STANDARD DMFs exist exist since differing nations have different regulations, such as LIGNOSPAN STANDARD USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A LIGNOSPAN STANDARD DMF submitted to regulatory agencies in the US is known as a USDMF. LIGNOSPAN STANDARD USDMF includes data on LIGNOSPAN STANDARD's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The LIGNOSPAN STANDARD USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of LIGNOSPAN STANDARD suppliers with USDMF on PharmaCompass.
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 LIGNOSPAN STANDARD Drug Master File in Japan (LIGNOSPAN STANDARD JDMF) empowers LIGNOSPAN STANDARD 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 LIGNOSPAN STANDARD JDMF during the approval evaluation for pharmaceutical products. At the time of LIGNOSPAN STANDARD JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of LIGNOSPAN STANDARD suppliers with JDMF on PharmaCompass.
In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a LIGNOSPAN STANDARD Drug Master File in Korea (LIGNOSPAN STANDARD KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of LIGNOSPAN STANDARD. The MFDS reviews the LIGNOSPAN STANDARD KDMF as part of the drug registration process and uses the information provided in the LIGNOSPAN STANDARD KDMF to evaluate the safety and efficacy of the drug.
After submitting a LIGNOSPAN STANDARD 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 LIGNOSPAN STANDARD API can apply through the Korea Drug Master File (KDMF).
click here to find a list of LIGNOSPAN STANDARD suppliers with KDMF on PharmaCompass.
A LIGNOSPAN STANDARD CEP of the European Pharmacopoeia monograph is often referred to as a LIGNOSPAN STANDARD Certificate of Suitability (COS). The purpose of a LIGNOSPAN STANDARD CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of LIGNOSPAN STANDARD EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of LIGNOSPAN STANDARD to their clients by showing that a LIGNOSPAN STANDARD CEP has been issued for it. The manufacturer submits a LIGNOSPAN STANDARD CEP (COS) as part of the market authorization procedure, and it takes on the role of a LIGNOSPAN STANDARD CEP holder for the record. Additionally, the data presented in the LIGNOSPAN STANDARD CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the LIGNOSPAN STANDARD DMF.
A LIGNOSPAN STANDARD CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. LIGNOSPAN STANDARD CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
click here to find a list of LIGNOSPAN STANDARD suppliers with CEP (COS) on PharmaCompass.
A LIGNOSPAN STANDARD written confirmation (LIGNOSPAN STANDARD WC) is an official document issued by a regulatory agency to a LIGNOSPAN STANDARD manufacturer, verifying that the manufacturing facility of a LIGNOSPAN STANDARD active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting LIGNOSPAN STANDARD APIs or LIGNOSPAN STANDARD finished pharmaceutical products to another nation, regulatory agencies frequently require a LIGNOSPAN STANDARD WC (written confirmation) as part of the regulatory process.
click here to find a list of LIGNOSPAN STANDARD suppliers with Written Confirmation (WC) on PharmaCompass.
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 LIGNOSPAN STANDARD as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for LIGNOSPAN STANDARD 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 LIGNOSPAN STANDARD 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 LIGNOSPAN STANDARD and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a LIGNOSPAN STANDARD NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of LIGNOSPAN STANDARD suppliers with NDC on PharmaCompass.
LIGNOSPAN STANDARD 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 LIGNOSPAN STANDARD 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 LIGNOSPAN STANDARD GMP manufacturer or LIGNOSPAN STANDARD GMP API supplier for your needs.
A LIGNOSPAN STANDARD CoA (Certificate of Analysis) is a formal document that attests to LIGNOSPAN STANDARD's compliance with LIGNOSPAN STANDARD specifications and serves as a tool for batch-level quality control.
LIGNOSPAN STANDARD CoA mostly includes findings from lab analyses of a specific batch. For each LIGNOSPAN STANDARD 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.
LIGNOSPAN STANDARD may be tested according to a variety of international standards, such as European Pharmacopoeia (LIGNOSPAN STANDARD EP), LIGNOSPAN STANDARD JP (Japanese Pharmacopeia) and the US Pharmacopoeia (LIGNOSPAN STANDARD USP).
