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01 1EUROAPI Germany GmbH

02 1AX Pharmaceutical Corp.

03 1BEC CHEMICALS PRIVATE LIMITED

04 1COSMA Spa

05 2Fagron Inc

06 1Galenova Inc

07 1KALCHEM INTERNATIONAL INC

08 2LETCO MEDICAL, LLC

09 1Medisca Inc

10 1Medisca Inc.

11 4Professional Compounding Centers of America

12 2Professional Compounding Centers of America dba PCCA

13 1Saurav Chemicals Limited

14 1Societa Italiana Medicinali Scandicci S.I.M.S., SrL

15 1Spectrum Laboratory Products, Inc.

16 1Village Pharma LLC

17 1Xenex Laboratories Inc

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PharmaCompass

01

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothEUROAPI, the leading small molecules API player, provides both API sales & CDMO services.

KETOPROFEN

NDC Package Code : 82348-102

Start Marketing Date : 2010-07-27

End Marketing Date : 2025-12-31

Dosage Form (Strength) : POWDER (1kg/kg)

Marketing Category : BULK INGREDIENT

EUROAPI Compnay Banner

02

Cophex
Not Confirmed
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Cophex
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KETOPROFEN

NDC Package Code : 51604-0011

Start Marketing Date : 2018-11-26

End Marketing Date : 2026-12-31

Dosage Form (Strength) : POWDER (1kg/kg)

Marketing Category : BULK INGREDIENT FOR HUMAN P...

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03

Cophex
Not Confirmed
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Cophex
Not Confirmed

KETOPROFEN

NDC Package Code : 51552-1501

Start Marketing Date : 2016-09-15

End Marketing Date : 2027-03-31

Dosage Form (Strength) : POWDER (1g/g)

Marketing Category : BULK INGREDIENT FOR HUMAN P...

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04

Cophex
Not Confirmed
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Cophex
Not Confirmed

KETOPROFEN

NDC Package Code : 51552-0307

Start Marketing Date : 2004-09-01

End Marketing Date : 2027-03-31

Dosage Form (Strength) : POWDER (1g/g)

Marketing Category : BULK INGREDIENT FOR HUMAN P...

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05

Cophex
Not Confirmed
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Cophex
Not Confirmed

KETOPROFEN

NDC Package Code : 38779-0078

Start Marketing Date : 2012-04-23

End Marketing Date : 2025-12-31

Dosage Form (Strength) : POWDER (1g/g)

Marketing Category : BULK INGREDIENT FOR HUMAN P...

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06

Cophex
Not Confirmed
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Cophex
Not Confirmed

KETOPROFEN

NDC Package Code : 38779-3039

Start Marketing Date : 2021-09-17

End Marketing Date : 2026-12-31

Dosage Form (Strength) : POWDER (1g/g)

Marketing Category : BULK INGREDIENT

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07

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Cophex
Not Confirmed

KETOPROFEN

NDC Package Code : 51927-0025

Start Marketing Date : 2018-01-05

End Marketing Date : 2025-08-31

Dosage Form (Strength) : POWDER (1kg/kg)

Marketing Category : BULK INGREDIENT FOR HUMAN P...

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08

Cophex
Not Confirmed
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Cophex
Not Confirmed

KETOPROFEN

NDC Package Code : 43235-0010

Start Marketing Date : 2018-01-01

End Marketing Date : 2025-12-31

Dosage Form (Strength) : POWDER (1kg/kg)

Marketing Category : DRUG FOR FURTHER PROCESSING

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09

Cophex
Not Confirmed
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Cophex
Not Confirmed

KETOPROFEN

NDC Package Code : 12660-0006

Start Marketing Date : 1979-02-01

End Marketing Date : 2025-12-31

Dosage Form (Strength) : POWDER (1kg/kg)

Marketing Category : BULK INGREDIENT

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10

Cophex
Not Confirmed
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Cophex
Not Confirmed

KETOPROFEN

NDC Package Code : 49452-3924

Start Marketing Date : 2017-12-01

End Marketing Date : 2025-12-31

Dosage Form (Strength) : POWDER (1g/g)

Marketing Category : BULK INGREDIENT

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Looking for 22071-15-4 / Ketoprofen API manufacturers, exporters & distributors?

Ketoprofen manufacturers, exporters & distributors 1

22

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

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

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

API | Excipient name

Ketoprofen

Synonyms

22071-15-4, 2-(3-benzoylphenyl)propanoic acid, Orudis, 2-(3-benzoylphenyl)propionic acid, Actron, Capisten

Cas Number

22071-15-4

Unique Ingredient Identifier (UNII)

90Y4QC304K

About Ketoprofen

An IBUPROFEN-type anti-inflammatory analgesic and antipyretic. It is used in the treatment of rheumatoid arthritis and osteoarthritis.

Actron Manufacturers

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

Actron Suppliers

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

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

Actron 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 Actron as an active pharmaceutical ingredient (API).

Finished drug products

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

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

Actron Manufacturers | Traders | Suppliers

Actron Manufacturers, Traders, Suppliers 1
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.