IOL Chemicals is an innovation-driven bulk drug, Intermediate and Specialty Chemicals company.
01 1IOL Chemicals and Pharmaceuticals Ltd.
02 1Wavelength Enterprises LTD
03 2Coprima SL
04 1Dasami Lab Private Limited
05 2Derivados Quimicos
06 3Harman Finochem Limited
07 1Hetero Drugs Limited
08 2Olon S.p.A.
09 2Olon SpA
10 1Pliva Croatia Ltd
11 1Spectrum Laboratory Products, Inc.
12 1Unichem Laboratories Limited, India
01 1FENOFIBRATE
02 12Fenofibrate
03 1Fenofibrate Micronized
04 1Fenofibrate micronized
05 2Fenofibric Acid
06 1fenofibrate
01 1Croatia
02 1France
03 7India
04 4Italy
05 4Spain
06 1U.S.A
IOL Chemicals is an innovation-driven bulk drug, Intermediate and Specialty Chemicals company.
NDC Package Code : 49716-330
Start Marketing Date : 2023-10-15
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients & provides custom-made solutions.
NDC Package Code : 58175-0348
Start Marketing Date : 2001-02-09
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Moehs Group, a reference company in the production of pharmaceutical active ingredients.
NDC Package Code : 68294-0001
Start Marketing Date : 2009-10-28
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Moehs Group, a reference company in the production of pharmaceutical active ingredients.
NDC Package Code : 68294-0002
Start Marketing Date : 2009-10-28
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 17337-0411
Start Marketing Date : 2017-12-12
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 17337-0019
Start Marketing Date : 2012-12-03
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 17337-0410
Start Marketing Date : 2017-05-17
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 17337-0430
Start Marketing Date : 2017-04-24
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 11722-065
Start Marketing Date : 2018-02-16
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (100kg/100kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 49452-3101
Start Marketing Date : 2019-12-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Fenofibrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Fenofibrate, including repackagers and relabelers. The FDA regulates Fenofibrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Fenofibrate 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 Fenofibrate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Fenofibrate supplier is an individual or a company that provides Fenofibrate active pharmaceutical ingredient (API) or Fenofibrate finished formulations upon request. The Fenofibrate suppliers may include Fenofibrate API manufacturers, exporters, distributors and traders.
click here to find a list of Fenofibrate 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 Fenofibrate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Fenofibrate 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 Fenofibrate 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 Fenofibrate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Fenofibrate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Fenofibrate suppliers with NDC on PharmaCompass.
We have 11 companies offering Fenofibrate
Get in contact with the supplier of your choice:
LOOKING FOR A SUPPLIER?
