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Also known as: 182349-12-8, Rupatadin fumarate, Rupafin, Ur-12592 fumarate, Rupatadine (fumarate), Alergoliber
Molecular Formula
C30H30ClN3O4
Molecular Weight
532.0  g/mol
InChI Key
JYBLCDXVHQWMSU-WLHGVMLRSA-N
FDA UNII
XJ6OT32M93

Rupatadine Fumarate
1 2D Structure

Rupatadine Fumarate

2 Identification
2.1 Computed Descriptors
2.1.1 IUPAC Name
(E)-but-2-enedioic acid;13-chloro-2-[1-[(5-methylpyridin-3-yl)methyl]piperidin-4-ylidene]-4-azatricyclo[9.4.0.03,8]pentadeca-1(11),3(8),4,6,12,14-hexaene
2.1.2 InChI
InChI=1S/C26H26ClN3.C4H4O4/c1-18-13-19(16-28-15-18)17-30-11-8-20(9-12-30)25-24-7-6-23(27)14-22(24)5-4-21-3-2-10-29-26(21)25;5-3(6)1-2-4(7)8/h2-3,6-7,10,13-16H,4-5,8-9,11-12,17H2,1H3;1-2H,(H,5,6)(H,7,8)/b;2-1+
2.1.3 InChI Key
JYBLCDXVHQWMSU-WLHGVMLRSA-N
2.1.4 Canonical SMILES
CC1=CC(=CN=C1)CN2CCC(=C3C4=C(CCC5=C3N=CC=C5)C=C(C=C4)Cl)CC2.C(=CC(=O)O)C(=O)O
2.1.5 Isomeric SMILES
CC1=CC(=CN=C1)CN2CCC(=C3C4=C(CCC5=C3N=CC=C5)C=C(C=C4)Cl)CC2.C(=C/C(=O)O)\C(=O)O
2.2 Other Identifiers
2.2.1 UNII
XJ6OT32M93
2.3 Synonyms
2.3.1 Depositor-Supplied Synonyms

1. 182349-12-8

2. Rupatadin Fumarate

3. Rupafin

4. Ur-12592 Fumarate

5. Rupatadine (fumarate)

6. Alergoliber

7. Rinialer

8. Xj6ot32m93

9. 182349-12-8 (fumarate)

10. Rupax

11. 8-chloro-11-(1-((5-methylpyridin-3-yl)methyl)piperidin-4-ylidene)-6,11-dihydro-5h-benzo[5,6]cyclohepta[1,2-b]pyridine Fumarate

12. Rupatadine Fumarate (jan)

13. 1217234-48-4

14. Rupatadine Fumarate [jan]

15. (2e)-but-2-enedioic Acid; 13-chloro-2-{1-[(5-methylpyridin-3-yl)methyl]piperidin-4-ylidene}-4-azatricyclo[9.4.0.0^{3,8}]pentadeca-1(15),3,5,7,11,13-hexaene

16. 5h-benzo[5,6]cyclohepta[1,2-b]pyridine, 8-chloro-6,11-dihydro-11-[1-[(5-methyl-3-pyridinyl)methyl]-4-piperidinylidene]-, (2e)-2-butenedioate (1:1)

17. Mfcd00926499

18. Unii-xj6ot32m93

19. Rupatall

20. Tamalis

21. Wystamm

22. Ralif

23. Rinialer (tn)

24. 5h-benzo(5,6)cyclohepta(1,2-b)pyridine, 8-chloro-6,11-dihydro-11-(1-((5-methyl-3-pyridinyl)methyl)-4-piperidinylidene)-, (2e)-2-butenedioate (1:1)

25. Rupafin (tn)

26. Rupatadine Fumarate- Bio-x

27. 5h-benzo(5,6)cyclohepta(1,2-b)pyridine, 6,11-dihydro-8-chloro-11-(1-((5-methyl-3-pyridinyl)methyl)-4-piperidinylidene)-, (e)-2-butenedioate (1:1)

28. 8-chloro-6,11-dihydro-11-[1-[(5-methyl-3-pyridyl)methyl]-4-piperidylidene]-5h-benzo[5,6]cyclohepta[1,2-b]pyridine Fumarate

29. Mls006010150

30. Schembl180121

31. Schembl180512

32. Rupatadine Fumarate [mi]

33. Hms3885k05

34. Bcp05230

35. Hy-13511a

36. Rupatadine Fumarate [who-dd]

37. S3052

38. Akos005145898

39. Ac-9016

40. Ccg-269922

41. Cs-3482

42. F76r825

43. Ks-1229

44. Br164385

45. Rupatadine Fumarate [ep Monograph]

46. Smr004701267

47. Sw219889-1

48. C73520

49. D08497

50. Q-201688

51. Q27293863

52. (e)-but-2-enedioic Acid;13-chloro-2-[1-[(5-methylpyridin-3-yl)methyl]piperidin-4-ylidene]-4-azatricyclo[9.4.0.03,8]pentadeca-1(11),3(8),4,6,12,14-hexaene

2.4 Create Date
2006-04-29
3 Chemical and Physical Properties
Molecular Weight 532.0 g/mol
Molecular Formula C30H30ClN3O4
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count7
Rotatable Bond Count4
Exact Mass531.1924841 g/mol
Monoisotopic Mass531.1924841 g/mol
Topological Polar Surface Area104 Ų
Heavy Atom Count38
Formal Charge0
Complexity728
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count1
Undefined Bond Stereocenter Count0
Covalently Bonded Unit Count2
4 Drug and Medication Information
4.1 Drug Indication

Treatment of allergic rhinitis, Treatment of chronic idiopathic urticaria


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07-Jan-2022
28-Apr-2025
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Looking for 182349-12-8 / Rupatadine Fumarate API manufacturers, exporters & distributors?

Rupatadine Fumarate manufacturers, exporters & distributors 1

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PharmaCompass offers a list of Rupatadine Fumarate 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 Rupatadine Fumarate manufacturer or Rupatadine Fumarate supplier for your needs.

Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Rupatadine Fumarate manufacturer or Rupatadine Fumarate supplier.

PharmaCompass also assists you with knowing the Rupatadine Fumarate API Price utilized in the formulation of products. Rupatadine Fumarate API Price is not always fixed or binding as the Rupatadine Fumarate Price is obtained through a variety of data sources. The Rupatadine Fumarate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.

API | Excipient name

Rupatadine Fumarate

Synonyms

182349-12-8, Rupatadin fumarate, Rupafin, Ur-12592 fumarate, Rupatadine (fumarate), Alergoliber

Cas Number

182349-12-8

Unique Ingredient Identifier (UNII)

XJ6OT32M93

Rupax Manufacturers

A Rupax manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Rupax, including repackagers and relabelers. The FDA regulates Rupax manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Rupax 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 Rupax manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

Rupax Suppliers

A Rupax supplier is an individual or a company that provides Rupax active pharmaceutical ingredient (API) or Rupax finished formulations upon request. The Rupax suppliers may include Rupax API manufacturers, exporters, distributors and traders.

click here to find a list of Rupax suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

Rupax USDMF

A Rupax DMF (Drug Master File) is a document detailing the whole manufacturing process of Rupax active pharmaceutical ingredient (API) in detail. Different forms of Rupax DMFs exist exist since differing nations have different regulations, such as Rupax USDMF, ASMF (EDMF), JDMF, CDMF, etc.

A Rupax DMF submitted to regulatory agencies in the US is known as a USDMF. Rupax USDMF includes data on Rupax's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Rupax USDMF is kept confidential to protect the manufacturer’s intellectual property.

click here to find a list of Rupax suppliers with USDMF on PharmaCompass.

Rupax JDMF

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 Rupax Drug Master File in Japan (Rupax JDMF) empowers Rupax 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 Rupax JDMF during the approval evaluation for pharmaceutical products. At the time of Rupax 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 Rupax suppliers with JDMF on PharmaCompass.

Rupax KDMF

In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.

Pharmaceutical companies submit a Rupax Drug Master File in Korea (Rupax KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Rupax. The MFDS reviews the Rupax KDMF as part of the drug registration process and uses the information provided in the Rupax KDMF to evaluate the safety and efficacy of the drug.

After submitting a Rupax 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 Rupax API can apply through the Korea Drug Master File (KDMF).

click here to find a list of Rupax suppliers with KDMF on PharmaCompass.

Rupax CEP

A Rupax CEP of the European Pharmacopoeia monograph is often referred to as a Rupax Certificate of Suitability (COS). The purpose of a Rupax CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Rupax EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Rupax to their clients by showing that a Rupax CEP has been issued for it. The manufacturer submits a Rupax CEP (COS) as part of the market authorization procedure, and it takes on the role of a Rupax CEP holder for the record. Additionally, the data presented in the Rupax CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Rupax DMF.

A Rupax CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Rupax 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 Rupax suppliers with CEP (COS) on PharmaCompass.

Rupax WC

A Rupax written confirmation (Rupax WC) is an official document issued by a regulatory agency to a Rupax manufacturer, verifying that the manufacturing facility of a Rupax active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Rupax APIs or Rupax finished pharmaceutical products to another nation, regulatory agencies frequently require a Rupax WC (written confirmation) as part of the regulatory process.

click here to find a list of Rupax suppliers with Written Confirmation (WC) on PharmaCompass.

Rupax NDC

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 Rupax as an active pharmaceutical ingredient (API).

Finished drug products

The FDA updates the NDC directory daily. The NDC numbers for Rupax API and other APIs are published in this directory by the FDA.

Unfinished drugs

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 Rupax 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.

Compounded drug products

The NDC directory also contains data on finished compounded human drug products that contain Rupax and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Rupax NDC to their finished compounded human drug products, they may choose to do so.

click here to find a list of Rupax suppliers with NDC on PharmaCompass.

Rupax GMP

Rupax 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 Rupax 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 Rupax GMP manufacturer or Rupax GMP API supplier for your needs.

Rupax CoA

A Rupax CoA (Certificate of Analysis) is a formal document that attests to Rupax's compliance with Rupax specifications and serves as a tool for batch-level quality control.

Rupax CoA mostly includes findings from lab analyses of a specific batch. For each Rupax 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.

Rupax may be tested according to a variety of international standards, such as European Pharmacopoeia (Rupax EP), Rupax JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Rupax USP).

Inform the supplier about your product requirements, specifying if you need a product with particular monograph like EP (Ph. Eur.), USP, JP, BP, or any other quality. In addition, clarify whether you need hydrochloride (HCl), anhydricum, base, micronisatum or a specific level of purity. To find reputable suppliers, utilize the filters and select those certified by GMP, FDA, or any other certification as per your requirement.
For your convenience, we have listed synonyms and CAS numbers to help you find the best supplier. The use of synonyms and CAS numbers can be helpful in identifying potential suppliers, but it is crucial to note that they might not always indicate the exact same product. It is important to confirm the product details with the supplier before making a purchase to ensure that it meets your requirements.
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