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1. Dihydrohydroxycodeinone
2. Dihydrone
3. Dinarkon
4. Eucodal
5. Oxiconum
6. Oxycodeinon
7. Oxycodone
8. Oxycone
9. Oxycontin
10. Pancodine
11. Theocodin
1. 124-90-3
2. Oxycodone Hcl
3. Oxecta
4. Oxycontin
5. Endocodone
6. Roxicodone
7. Oxycodone Hydrochloride Cii
8. Chebi:7859
9. 4,5alpha-epoxy-14-hydroxy-3-methoxy-17-methylmorphinan-6-one Hydrochloride
10. (4r,4as,7ar,12bs)-4a-hydroxy-9-methoxy-3-methyl-2,4,5,6,7a,13-hexahydro-1h-4,12-methanobenzofuro[3,2-e]isoquinolin-7-one;hydrochloride
11. (4r,4as,7ar,12bs)-4a-hydroxy-9-methoxy-3-methyl-2,4,5,6,7a,13-hexahydro-1h-4,12-methanobenzofuro[3,2-e]isoquinolin-7-one;hydron;chloride
12. Roxicodone (tn)
13. Oxycontin (tn)
14. (4r,4as,7ar,12bs)-4a-hydroxy-9-methoxy-3-methyl-2,4,5,6,7a,13-hexahydro-1h-4,12-methanobenzofuro[3,2-e]isoquinoline-7-one;hydrochloride
15. Oxecta (tn)
16. Roxybond
17. Oxycodone Monohydrochloride
18. Schembl30095
19. Oxycodone Hydrochloride (usp)
20. Chembl1200890
21. Dtxsid80924674
22. Oxycodone Hydrochloride [mi]
23. Oxycodone Hydrochloride [usan]
24. Akos024457896
25. Oxycodone Hydrochloride [mart.]
26. Oxycodone Hydrochloride [vandf]
27. Anhydrous Oxycodone Hydrochloride
28. Oxycodone Hydrochloride [who-dd]
29. Oxycodone Hydrochloride, Analytical Standard
30. Oxycodone Hydrochloride [orange Book]
31. Oxycodone Hydrochloride Cii [usp-rs]
32. Oxycodone Hydrochloride [ep Monograph]
33. Tylox Component Oxycodone Hydrochloride
34. C08026
35. Codoxy Component Oxycodone Hydrochloride
36. D00847
37. Oxycet Component Oxycodone Hydrochloride
38. Oxycodone Hydrochloride [usp Monograph]
39. Roxicet Component Oxycodone Hydrochloride
40. Roxilox Component Oxycodone Hydrochloride
41. Troxyca Component Oxycodone Hydrochloride
42. Combunox Component Oxycodone Hydrochloride
43. Oxycodone Hydrochloride Component Of Tylox
44. Percocet Component Oxycodone Hydrochloride
45. Percodan Component Oxycodone Hydrochloride
46. Roxiprin Component Oxycodone Hydrochloride
47. Targiniq Component Oxycodone Hydrochloride
48. Xartemis Component Oxycodone Hydrochloride
49. Oxycodone Hydrochloride Component Of Codoxy
50. Oxycodone Hydrochloride Component Of Oxycet
51. Oxycodone Hydrochloride Component Of Roxicet
52. Oxycodone Hydrochloride Component Of Roxilox
53. Oxycodone Hydrochloride Component Of Troxyca
54. Oxycodone Hydrochloride Component Of Combunox
55. Oxycodone Hydrochloride Component Of Percocet
56. Oxycodone Hydrochloride Component Of Percodan
57. Oxycodone Hydrochloride Component Of Roxiprin
58. Oxycodone Hydrochloride Component Of Targiniq
59. Oxycodone Hydrochloride Component Of Xartemis
60. Percodan-demi Component Oxycodone Hydrochloride
61. Q27107601
62. Oxycodone Hydrochloride Component Of Percodan-demi
63. 14-hydroxy-3-methoxy-17-methyl-4,5alpha-epoxymorphinan-6-one Hydrochloride
64. Oxycodone Hydrochloride, European Pharmacopoeia (ep) Reference Standard
65. Oxycodone Hydrochloride, United States Pharmacopeia (usp) Reference Standard
66. (5?)-4,5-epoxy-14-hydroxy-3-methoxy-17-methylmorphinan-6-one Hydrochloride
67. (5alpha,17s)-14-hydroxy-3-methoxy-17-methyl-6-oxo-4,5-epoxymorphinan-17-ium Chloride
68. 4,5.alpha.-epoxy-14-hydroxy-3-methoxy-17-methylmorphinan-6-one Hydrochloride
69. Morphinan-6-one, 4,5-epoxy-14-hydroxy-3-methoxy-17-methyl-, Hydrochloride, (5.alpha.)-
70. Oxycodone Hydrochloride Solution, 1.0 Mg/ml In Methanol, Analytical Standard, For Drug Analysis
Molecular Weight | 351.8 g/mol |
---|---|
Molecular Formula | C18H22ClNO4 |
Hydrogen Bond Donor Count | 2 |
Hydrogen Bond Acceptor Count | 5 |
Rotatable Bond Count | 1 |
Exact Mass | 351.1237359 g/mol |
Monoisotopic Mass | 351.1237359 g/mol |
Topological Polar Surface Area | 59 Ų |
Heavy Atom Count | 24 |
Formal Charge | 0 |
Complexity | 553 |
Isotope Atom Count | 0 |
Defined Atom Stereocenter Count | 4 |
Undefined Atom Stereocenter Count | 0 |
Defined Bond Stereocenter Count | 0 |
Undefined Bond Stereocenter Count | 0 |
Covalently Bonded Unit Count | 2 |
1 of 4 | |
---|---|
Drug Name | Oxecta |
Drug Label | OXECTA (oxycodone HCl, USP) tablets are an immediate-release opioid analgesic intended for oral administration only. OXECTA contains oxycodone HCl, USP as the active analgesic ingredient. The tablets are round, convex, white and debossed with the str... |
Active Ingredient | Oxycodone hydrochloride |
Dosage Form | Tablet |
Route | Oral |
Strength | 7.5mg; 5mg |
Market Status | Prescription |
Company | Acura Pharms |
2 of 4 | |
---|---|
Drug Name | Oxycodone hydrochloride |
Drug Label | DESCRIPTIONOxyContin (oxycodone hydrochloride controlled-release) Tablets are an opioid analgesic supplied in 10 mg, 15 mg, 20 mg, 30 mg, 40 mg, 60 mg, 80 mg, and 160 mg tablet strengths for oral administration... |
Active Ingredient | Oxycodone hydrochloride |
Dosage Form | Tablet, extended release; Tablet; Capsule; Solution |
Route | oral; Oral |
Strength | 30mg; 100mg/5ml; 15mg; 5mg; 10mg; 5mg/5ml; 80mg; 40mg; 20mg |
Market Status | Tentative Approval; Prescription |
Company | Corepharma; Vintage Pharms; Amneal Pharms; Impax Pharms; Aurolife Pharma; Avanthi; Teva; Endo Pharms; Sun Pharm Inds; Coastal Pharms; Rhodes Pharms; Mallinckrodt; Roxane; Lannett Holdings; Nesher Pharms; Vistapharm; Actavis Elizabeth; Lehigh Valley; Alvog |
3 of 4 | |
---|---|
Drug Name | Oxecta |
Drug Label | OXECTA (oxycodone HCl, USP) tablets are an immediate-release opioid analgesic intended for oral administration only. OXECTA contains oxycodone HCl, USP as the active analgesic ingredient. The tablets are round, convex, white and debossed with the str... |
Active Ingredient | Oxycodone hydrochloride |
Dosage Form | Tablet |
Route | Oral |
Strength | 7.5mg; 5mg |
Market Status | Prescription |
Company | Acura Pharms |
4 of 4 | |
---|---|
Drug Name | Oxycodone hydrochloride |
Drug Label | DESCRIPTIONOxyContin (oxycodone hydrochloride controlled-release) Tablets are an opioid analgesic supplied in 10 mg, 15 mg, 20 mg, 30 mg, 40 mg, 60 mg, 80 mg, and 160 mg tablet strengths for oral administration... |
Active Ingredient | Oxycodone hydrochloride |
Dosage Form | Tablet, extended release; Tablet; Capsule; Solution |
Route | oral; Oral |
Strength | 30mg; 100mg/5ml; 15mg; 5mg; 10mg; 5mg/5ml; 80mg; 40mg; 20mg |
Market Status | Tentative Approval; Prescription |
Company | Corepharma; Vintage Pharms; Amneal Pharms; Impax Pharms; Aurolife Pharma; Avanthi; Teva; Endo Pharms; Sun Pharm Inds; Coastal Pharms; Rhodes Pharms; Mallinckrodt; Roxane; Lannett Holdings; Nesher Pharms; Vistapharm; Actavis Elizabeth; Lehigh Valley; Alvog |
Analgesics, Opioid
Compounds with activity like OPIATE ALKALOIDS, acting at OPIOID RECEPTORS. Properties include induction of ANALGESIA or NARCOSIS. (See all compounds classified as Analgesics, Opioid.)
Narcotics
Agents that induce NARCOSIS. Narcotics include agents that cause somnolence or induced sleep (STUPOR); natural or synthetic derivatives of OPIUM or MORPHINE or any substance that has such effects. They are potent inducers of ANALGESIA and OPIOID-RELATED DISORDERS. (See all compounds classified as Narcotics.)
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Importing Country | Total Quantity (KGS) |
Average Price (USD/KGS) |
Number of Transactions |
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PharmaCompass offers a list of Oxycodone Hydrochloride 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 Oxycodone Hydrochloride manufacturer or Oxycodone Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Oxycodone Hydrochloride manufacturer or Oxycodone Hydrochloride supplier.
PharmaCompass also assists you with knowing the Oxycodone Hydrochloride API Price utilized in the formulation of products. Oxycodone Hydrochloride API Price is not always fixed or binding as the Oxycodone Hydrochloride Price is obtained through a variety of data sources. The Oxycodone Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Eucodal manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Eucodal, including repackagers and relabelers. The FDA regulates Eucodal manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Eucodal 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 Eucodal manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Eucodal supplier is an individual or a company that provides Eucodal active pharmaceutical ingredient (API) or Eucodal finished formulations upon request. The Eucodal suppliers may include Eucodal API manufacturers, exporters, distributors and traders.
click here to find a list of Eucodal suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Eucodal DMF (Drug Master File) is a document detailing the whole manufacturing process of Eucodal active pharmaceutical ingredient (API) in detail. Different forms of Eucodal DMFs exist exist since differing nations have different regulations, such as Eucodal USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Eucodal DMF submitted to regulatory agencies in the US is known as a USDMF. Eucodal USDMF includes data on Eucodal's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Eucodal USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Eucodal 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 Eucodal Drug Master File in Japan (Eucodal JDMF) empowers Eucodal 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 Eucodal JDMF during the approval evaluation for pharmaceutical products. At the time of Eucodal 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 Eucodal 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 Eucodal Drug Master File in Korea (Eucodal KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Eucodal. The MFDS reviews the Eucodal KDMF as part of the drug registration process and uses the information provided in the Eucodal KDMF to evaluate the safety and efficacy of the drug.
After submitting a Eucodal 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 Eucodal API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Eucodal suppliers with KDMF on PharmaCompass.
A Eucodal CEP of the European Pharmacopoeia monograph is often referred to as a Eucodal Certificate of Suitability (COS). The purpose of a Eucodal CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Eucodal EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Eucodal to their clients by showing that a Eucodal CEP has been issued for it. The manufacturer submits a Eucodal CEP (COS) as part of the market authorization procedure, and it takes on the role of a Eucodal CEP holder for the record. Additionally, the data presented in the Eucodal CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Eucodal DMF.
A Eucodal CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Eucodal 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 Eucodal suppliers with CEP (COS) on PharmaCompass.
A Eucodal written confirmation (Eucodal WC) is an official document issued by a regulatory agency to a Eucodal manufacturer, verifying that the manufacturing facility of a Eucodal active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Eucodal APIs or Eucodal finished pharmaceutical products to another nation, regulatory agencies frequently require a Eucodal WC (written confirmation) as part of the regulatory process.
click here to find a list of Eucodal 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 Eucodal as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Eucodal 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 Eucodal 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 Eucodal and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Eucodal NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Eucodal suppliers with NDC on PharmaCompass.
Eucodal 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 Eucodal 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 Eucodal GMP manufacturer or Eucodal GMP API supplier for your needs.
A Eucodal CoA (Certificate of Analysis) is a formal document that attests to Eucodal's compliance with Eucodal specifications and serves as a tool for batch-level quality control.
Eucodal CoA mostly includes findings from lab analyses of a specific batch. For each Eucodal 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.
Eucodal may be tested according to a variety of international standards, such as European Pharmacopoeia (Eucodal EP), Eucodal JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Eucodal USP).