01 1Bozhou Kunyu Biotechnology Co., Ltd.
02 1Catalent Micron Technologies, Inc.
03 1DARMERICA, LLC
04 1Fagron Inc
05 1Genvion Corporation
06 2IMCD Switzerland AG
07 1Jetpharma S.A.
08 1LETCO MEDICAL, LLC
09 1MEDISCA Inc.
10 1Medisca Inc.
11 1Nantong Jinghua Pharmaceutical Co., Ltd.
12 1Professional Compounding Centers of America dba PCCA
13 1Sicor de Mexico S.A. de C.V
14 1Spectrum Laboratory Products, Inc.
01 55-Fluorouracil
02 3FLUOROURACIL
03 5Fluorouracil
04 1Fluorouracil-5
05 1Fluorourcil
01 1Canada
02 1China
03 1Mexico
04 3Netherlands
05 1Switzerland
06 6U.S.A
07 1United Kingdom
08 1Blank
NDC Package Code : 51552-0733
Start Marketing Date : 1998-04-01
End Marketing Date : 2025-01-08
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 62049-185
Start Marketing Date : 2019-05-07
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 12070-0001
Start Marketing Date : 2017-01-23
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 12070-0002
Start Marketing Date : 2017-10-21
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 62991-1486
Start Marketing Date : 2010-12-13
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 38779-0025
Start Marketing Date : 2011-05-10
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 38779-3185
Start Marketing Date : 2019-05-07
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 59348-0055
Start Marketing Date : 1982-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51927-1085
Start Marketing Date : 2013-06-24
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 49452-3175
Start Marketing Date : 1997-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
A Fluorouracil manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Fluorouracil, including repackagers and relabelers. The FDA regulates Fluorouracil manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Fluorouracil 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 Fluorouracil manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Fluorouracil supplier is an individual or a company that provides Fluorouracil active pharmaceutical ingredient (API) or Fluorouracil finished formulations upon request. The Fluorouracil suppliers may include Fluorouracil API manufacturers, exporters, distributors and traders.
click here to find a list of Fluorouracil 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 Fluorouracil as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Fluorouracil 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 Fluorouracil 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 Fluorouracil and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Fluorouracil NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Fluorouracil suppliers with NDC on PharmaCompass.
We have 12 companies offering Fluorouracil
Get in contact with the supplier of your choice:
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