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Chemistry

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Also known as: 15307-81-0, Cataflam, Cgp 45840b, Voltfast, Cambia, Zipsor
Molecular Formula
C14H10Cl2KNO2
Molecular Weight
334.2  g/mol
InChI Key
KXZOIWWTXOCYKR-UHFFFAOYSA-M
FDA UNII
L4D5UA6CB4

Diclofenac Potassium
A non-steroidal anti-inflammatory agent (NSAID) with antipyretic and analgesic actions. It is primarily available as the sodium salt.
1 2D Structure

Diclofenac Potassium

2 Identification
2.1 Computed Descriptors
2.1.1 IUPAC Name
potassium;2-[2-(2,6-dichloroanilino)phenyl]acetate
2.1.2 InChI
InChI=1S/C14H11Cl2NO2.K/c15-10-5-3-6-11(16)14(10)17-12-7-2-1-4-9(12)8-13(18)19;/h1-7,17H,8H2,(H,18,19);/q;+1/p-1
2.1.3 InChI Key
KXZOIWWTXOCYKR-UHFFFAOYSA-M
2.1.4 Canonical SMILES
C1=CC=C(C(=C1)CC(=O)[O-])NC2=C(C=CC=C2Cl)Cl.[K+]
2.2 Other Identifiers
2.2.1 UNII
L4D5UA6CB4
2.3 Synonyms
2.3.1 MeSH Synonyms

1. Dichlofenal

2. Diclofenac

3. Diclofenac Sodium

4. Diclofenac, Sodium

5. Diclonate P

6. Diclophenac

7. Dicrofenac

8. Feloran

9. Gp 45,840

10. Gp-45,840

11. Gp45,840

12. Novapirina

13. Orthofen

14. Orthophen

15. Ortofen

16. Sodium Diclofenac

17. Sr 38

18. Sr-38

19. Sr38

20. Voltaren

21. Voltarol

2.3.2 Depositor-Supplied Synonyms

1. 15307-81-0

2. Cataflam

3. Cgp 45840b

4. Voltfast

5. Cambia

6. Zipsor

7. Diclofenac Potassium [usan:usp]

8. Potassium Diclofenac

9. Potassium;2-[2-(2,6-dichloroanilino)phenyl]acetate

10. Diclofenac (potassium)

11. Cgp-45840b

12. Diclofenac Potassium Salt

13. L4d5ua6cb4

14. Chebi:4508

15. Benzeneacetic Acid, 2-((2,6-dichlorophenyl)amino)-, Monopotassium Salt

16. Potassium 2-(2-((2,6-dichlorophenyl)amino)phenyl)acetate

17. Cataflam; Diclofenac Potassium; K-fenak; Potassium Diclofenac; Prosorb

18. Diclofenac Potassium [usan]

19. Unii-l4d5ua6cb4

20. Cataflam (tn)

21. Potassium (o-(2,6-dichloroanilino)phenyl)acetate

22. Cambia (tn)

23. Zipsor (tn)

24. Diclofenac Potassium (usp)

25. Schembl40784

26. Chembl1200804

27. Dtxsid30165212

28. Hms3656d18

29. Diclofenac Potassium [vandf]

30. Diclofenac Potassium [mart.]

31. S3062

32. Diclofenac Potassium [usp-rs]

33. Diclofenac Potassium [who-dd]

34. Akos015889752

35. Akos015994733

36. Diclofenac Potassium Salt [mi]

37. Ccg-267848

38. Ks-5037

39. Ac-18735

40. Diclofenac Potassium [orange Book]

41. Hy-15038

42. Diclofenac Potassium [ep Monograph]

43. Db-043176

44. Diclofenac Potassium [usp Monograph]

45. Cs-0003712

46. Ft-0603076

47. Sw196404-4

48. D00903

49. Q27106401

50. Potassium {2-[(2,6-dichlorophenyl)amino]phenyl}acetate

51. Potassium 2-(2-(2,6-dichlorophenylamino)phenyl)acetate

52. Potassium (o-((2,6-dichlorophenyl)amino)phenyl)acetate

53. 2-((2,6-dichlorophenyl)amino)benzeneacetic Acid, Monopotassium Salt

2.4 Create Date
2008-02-05
3 Chemical and Physical Properties
Molecular Weight 334.2 g/mol
Molecular Formula C14H10Cl2KNO2
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count3
Rotatable Bond Count4
Exact Mass332.9725654 g/mol
Monoisotopic Mass332.9725654 g/mol
Topological Polar Surface Area52.2 Ų
Heavy Atom Count20
Formal Charge0
Complexity310
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
Covalently Bonded Unit Count2
4 Drug and Medication Information
4.1 Drug Information
1 of 8  
Drug NameCambia
Drug LabelCAMBIA (Diclofenac Potassium for Oral Solution) is a benzeneacetic acid derivative NSAID. CAMBIA is available as a buffered soluble powder, designed to be mixed with water prior to oral administration. CAMBIA is a white to off-white, buff...
Active IngredientDiclofenac potassium
Dosage FormFor solution
RouteOral
Strength50mg
Market StatusPrescription
CompanyDepomed

2 of 8  
Drug NameCataflam
PubMed HealthDiclofenac
Drug ClassesAnalgesic, Anti-Inflammatory, Antimigraine, Antirheumatic, Central Nervous System Agent, Musculoskeletal Agent, Ophthalmologic Agent
Drug LabelCataflam (diclofenac potassium immediate-release tablets) is a benzeneacetic acid derivative. Cataflam is available as immediate-release tablets of 50 mg (light brown) for oral administration. The chemical name is 2-[(2,6-dichlorophenyl)amino] benz...
Active IngredientDiclofenac potassium
Dosage FormTablet
RouteOral
Strength50mg
Market StatusPrescription
CompanyNovartis

3 of 8  
Drug NameDiclofenac potassium
Drug LabelDiclofenac potassium tablets USP are a benzeneacetic acid derivative. Diclofenac potassium tablets USP, 50 mg are available as orange, film-coated tablets for oral administration. The chemical name is 2-[(2,6-dichlorophenyl)amino] benzeneacetic acid,...
Active IngredientDiclofenac potassium
Dosage FormTablet
RouteOral
Strength50mg
Market StatusPrescription
CompanyTeva; Apotex; Sandoz; Mylan

4 of 8  
Drug NameZipsor
PubMed HealthDiclofenac
Drug ClassesAnalgesic, Anti-Inflammatory, Antimigraine, Antirheumatic, Central Nervous System Agent, Musculoskeletal Agent, Ophthalmologic Agent
Drug LabelZipsor (diclofenac potassium) Liquid Filled Capsule is a benzeneacetic acid derivative NSAID. Zipsor is available as liquid-filled capsules of 25 mg for oral administration. The chemical name is 2-[(2,6- dichlorophenyl) amino] benzeneacetic acid mono...
Active IngredientDiclofenac potassium
Dosage FormCapsule
RouteOral
Strength25mg
Market StatusPrescription
CompanyDepomed

5 of 8  
Drug NameCambia
Drug LabelCAMBIA (Diclofenac Potassium for Oral Solution) is a benzeneacetic acid derivative NSAID. CAMBIA is available as a buffered soluble powder, designed to be mixed with water prior to oral administration. CAMBIA is a white to off-white, buff...
Active IngredientDiclofenac potassium
Dosage FormFor solution
RouteOral
Strength50mg
Market StatusPrescription
CompanyDepomed

6 of 8  
Drug NameCataflam
PubMed HealthDiclofenac
Drug ClassesAnalgesic, Anti-Inflammatory, Antimigraine, Antirheumatic, Central Nervous System Agent, Musculoskeletal Agent, Ophthalmologic Agent
Drug LabelCataflam (diclofenac potassium immediate-release tablets) is a benzeneacetic acid derivative. Cataflam is available as immediate-release tablets of 50 mg (light brown) for oral administration. The chemical name is 2-[(2,6-dichlorophenyl)amino] benz...
Active IngredientDiclofenac potassium
Dosage FormTablet
RouteOral
Strength50mg
Market StatusPrescription
CompanyNovartis

7 of 8  
Drug NameDiclofenac potassium
Drug LabelDiclofenac potassium tablets USP are a benzeneacetic acid derivative. Diclofenac potassium tablets USP, 50 mg are available as orange, film-coated tablets for oral administration. The chemical name is 2-[(2,6-dichlorophenyl)amino] benzeneacetic acid,...
Active IngredientDiclofenac potassium
Dosage FormTablet
RouteOral
Strength50mg
Market StatusPrescription
CompanyTeva; Apotex; Sandoz; Mylan

8 of 8  
Drug NameZipsor
PubMed HealthDiclofenac
Drug ClassesAnalgesic, Anti-Inflammatory, Antimigraine, Antirheumatic, Central Nervous System Agent, Musculoskeletal Agent, Ophthalmologic Agent
Drug LabelZipsor (diclofenac potassium) Liquid Filled Capsule is a benzeneacetic acid derivative NSAID. Zipsor is available as liquid-filled capsules of 25 mg for oral administration. The chemical name is 2-[(2,6- dichlorophenyl) amino] benzeneacetic acid mono...
Active IngredientDiclofenac potassium
Dosage FormCapsule
RouteOral
Strength25mg
Market StatusPrescription
CompanyDepomed

5 Pharmacology and Biochemistry
5.1 MeSH Pharmacological Classification

Anti-Inflammatory Agents, Non-Steroidal

Anti-inflammatory agents that are non-steroidal in nature. In addition to anti-inflammatory actions, they have analgesic, antipyretic, and platelet-inhibitory actions. They act by blocking the synthesis of prostaglandins by inhibiting cyclooxygenase, which converts arachidonic acid to cyclic endoperoxides, precursors of prostaglandins. Inhibition of prostaglandin synthesis accounts for their analgesic, antipyretic, and platelet-inhibitory actions; other mechanisms may contribute to their anti-inflammatory effects. (See all compounds classified as Anti-Inflammatory Agents, Non-Steroidal.)


Cyclooxygenase Inhibitors

Compounds or agents that combine with cyclooxygenase (PROSTAGLANDIN-ENDOPEROXIDE SYNTHASES) and thereby prevent its substrate-enzyme combination with arachidonic acid and the formation of eicosanoids, prostaglandins, and thromboxanes. (See all compounds classified as Cyclooxygenase Inhibitors.)


5.2 FDA Pharmacological Classification
5.2.1 Pharmacological Classes
Cyclooxygenase Inhibitors [MoA]; Decreased Prostaglandin Production [PE]; Nonsteroidal Anti-inflammatory Drug [EPC]; Anti-Inflammatory Agents, Non-Steroidal [CS]

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RIVOLTANA KM 6\/7 20053 RODANO (MI) Milano, , Italy Italy","customerAddress":"102,TITAN HOUSE,60 FEET RD,"}]
03-Jan-2022
30-May-2025
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DOSAGE - TABLET;ORAL - 25MG **Federal Registe...DOSAGE - TABLET;ORAL - 25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

USFDA APPLICATION NUMBER - 20142

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DOSAGE - TABLET;ORAL - 50MG **Federal Registe...DOSAGE - TABLET;ORAL - 50MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

USFDA APPLICATION NUMBER - 20142

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DOSAGE - CAPSULE;ORAL - 25MG

USFDA APPLICATION NUMBER - 22202

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ABOUT THIS PAGE

Looking for 15307-81-0 / Diclofenac Potassium API manufacturers, exporters & distributors?

Diclofenac Potassium manufacturers, exporters & distributors 1

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PharmaCompass offers a list of Diclofenac Potassium 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 Diclofenac Potassium manufacturer or Diclofenac Potassium supplier for your needs.

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

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

API | Excipient name

Diclofenac Potassium

Synonyms

15307-81-0, Cataflam, Cgp 45840b, Voltfast, Cambia, Zipsor

Cas Number

15307-81-0

Unique Ingredient Identifier (UNII)

L4D5UA6CB4

About Diclofenac Potassium

A non-steroidal anti-inflammatory agent (NSAID) with antipyretic and analgesic actions. It is primarily available as the sodium salt.

Cambia (TN) Manufacturers

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

Cambia (TN) Suppliers

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

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

Cambia (TN) USDMF

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

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

click here to find a list of Cambia (TN) suppliers with USDMF on PharmaCompass.

Cambia (TN) KDMF

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

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

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

click here to find a list of Cambia (TN) suppliers with KDMF on PharmaCompass.

Cambia (TN) CEP

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

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

Cambia (TN) WC

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

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

Cambia (TN) 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 Cambia (TN) as an active pharmaceutical ingredient (API).

Finished drug products

The FDA updates the NDC directory daily. The NDC numbers for Cambia (TN) 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 Cambia (TN) 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 Cambia (TN) and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Cambia (TN) NDC to their finished compounded human drug products, they may choose to do so.

click here to find a list of Cambia (TN) suppliers with NDC on PharmaCompass.

Cambia (TN) GMP

Cambia (TN) 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 Cambia (TN) 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 Cambia (TN) GMP manufacturer or Cambia (TN) GMP API supplier for your needs.

Cambia (TN) CoA

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

Cambia (TN) CoA mostly includes findings from lab analyses of a specific batch. For each Cambia (TN) 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.

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