01 1Aurobindo Pharma Limited
02 1MSN Laboratories Private Limited
03 1NATCO PHARMA LIMITED
04 1PHARMA WALDHOF GMBH
05 1Sionc Pharmaceutical Private Limited
06 1Yuki Gosei Kogyo Co., Ltd.
01 2TRIFLURIDINE
02 1Trifluorothymidine (Trifluridine/F3TDR)
03 2Trifluridine
04 1trifluridine
01 4India
02 1Japan
03 1U.S.A
NDC Package Code : 12562-0001
Start Marketing Date : 2012-01-01
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 59651-388
Start Marketing Date : 2024-01-11
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 54893-0086
Start Marketing Date : 2019-02-18
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 70225-1108
Start Marketing Date : 2018-05-02
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 76055-0037
Start Marketing Date : 2018-05-22
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 12785-0004
Start Marketing Date : 1997-01-01
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (500g/500g)
Marketing Category : BULK INGREDIENT
A Trifluridine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Trifluridine, including repackagers and relabelers. The FDA regulates Trifluridine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Trifluridine 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 Trifluridine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Trifluridine supplier is an individual or a company that provides Trifluridine active pharmaceutical ingredient (API) or Trifluridine finished formulations upon request. The Trifluridine suppliers may include Trifluridine API manufacturers, exporters, distributors and traders.
click here to find a list of Trifluridine 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 Trifluridine as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Trifluridine 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 Trifluridine 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 Trifluridine and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Trifluridine NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Trifluridine suppliers with NDC on PharmaCompass.
We have 6 companies offering Trifluridine
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