01 1Zhejiang ChemPacific Corporation
01 1Floxuridine
01 1U.S.A
NDC Package Code : 59981-052
Start Marketing Date : 2025-04-28
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Floxuridine 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 Floxuridine manufacturer or Floxuridine supplier for your needs.
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PharmaCompass also assists you with knowing the Floxuridine API Price utilized in the formulation of products. Floxuridine API Price is not always fixed or binding as the Floxuridine Price is obtained through a variety of data sources. The Floxuridine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A 039LU44I5M manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 039LU44I5M, including repackagers and relabelers. The FDA regulates 039LU44I5M manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 039LU44I5M API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A 039LU44I5M supplier is an individual or a company that provides 039LU44I5M active pharmaceutical ingredient (API) or 039LU44I5M finished formulations upon request. The 039LU44I5M suppliers may include 039LU44I5M API manufacturers, exporters, distributors and traders.
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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 039LU44I5M as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for 039LU44I5M 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 039LU44I5M 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 039LU44I5M and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a 039LU44I5M NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of 039LU44I5M suppliers with NDC on PharmaCompass.
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