01 1Fagron Inc
01 1Xylitol
01 1Netherlands
NDC Package Code : 51552-0754
Start Marketing Date : 2004-09-01
End Marketing Date : 2026-03-21
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
A Xylitol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Xylitol, including repackagers and relabelers. The FDA regulates Xylitol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Xylitol 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 Xylitol manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Xylitol supplier is an individual or a company that provides Xylitol active pharmaceutical ingredient (API) or Xylitol finished formulations upon request. The Xylitol suppliers may include Xylitol API manufacturers, exporters, distributors and traders.
click here to find a list of Xylitol 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 Xylitol as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Xylitol 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 Xylitol 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 Xylitol and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Xylitol NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Xylitol suppliers with NDC on PharmaCompass.
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