EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
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
01 12KETOPROFEN
02 1KETOPROFEN SPECIAL MICRONIZED
03 8Ketoprofen
04 1Ketoprofen Micronized
05 1Ketoprofen Ultra
01 3Canada
02 1France
03 2India
04 2Italy
05 1Latvia
06 2Netherlands
07 6U.S.A
08 6United Kingdom
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
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
NDC Package Code : 51604-0011
Start Marketing Date : 2018-11-26
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
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...
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...
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...
NDC Package Code : 38779-3039
Start Marketing Date : 2021-09-17
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
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...
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
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
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
A Ketoprofen manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ketoprofen, including repackagers and relabelers. The FDA regulates Ketoprofen manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ketoprofen 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 Ketoprofen manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ketoprofen supplier is an individual or a company that provides Ketoprofen active pharmaceutical ingredient (API) or Ketoprofen finished formulations upon request. The Ketoprofen suppliers may include Ketoprofen API manufacturers, exporters, distributors and traders.
click here to find a list of Ketoprofen suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information 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 Ketoprofen as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Ketoprofen 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 Ketoprofen 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 Ketoprofen and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Ketoprofen NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Ketoprofen suppliers with NDC on PharmaCompass.
We have 15 companies offering Ketoprofen
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