Moehs Group, a reference company in the production of pharmaceutical active ingredients.
01 1Coprima SL
02 1Curia Missouri, Inc.
03 1Glenmark Life Sciences Limited
04 1Harman Finochem Limited
05 1Olon S.p.A.
06 2Olon SpA
01 2CHOLINE FENOFIBRATE
02 5Choline Fenofibrate
01 2India
02 3Italy
03 1Spain
04 1U.S.A
Moehs Group, a reference company in the production of pharmaceutical active ingredients.
NDC Package Code : 68294-0003
Start Marketing Date : 2009-07-21
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 66039-874
Start Marketing Date : 2011-08-12
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 17180-0201
Start Marketing Date : 2012-06-26
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 66064-1007
Start Marketing Date : 2009-10-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 17337-0013
Start Marketing Date : 2012-12-27
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 17337-0042
Start Marketing Date : 2012-12-27
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 17337-0412
Start Marketing Date : 2017-12-12
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Choline Fenofibrate 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 Choline Fenofibrate manufacturer or Choline Fenofibrate supplier for your needs.
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PharmaCompass also assists you with knowing the Choline Fenofibrate API Price utilized in the formulation of products. Choline Fenofibrate API Price is not always fixed or binding as the Choline Fenofibrate Price is obtained through a variety of data sources. The Choline Fenofibrate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A TRILIPIX manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of TRILIPIX, including repackagers and relabelers. The FDA regulates TRILIPIX manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. TRILIPIX 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 TRILIPIX manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A TRILIPIX supplier is an individual or a company that provides TRILIPIX active pharmaceutical ingredient (API) or TRILIPIX finished formulations upon request. The TRILIPIX suppliers may include TRILIPIX API manufacturers, exporters, distributors and traders.
click here to find a list of TRILIPIX 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 TRILIPIX as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for TRILIPIX 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 TRILIPIX 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 TRILIPIX and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a TRILIPIX NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of TRILIPIX suppliers with NDC on PharmaCompass.
We have 5 companies offering TRILIPIX
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