01 1ACS Dobfar S.p.A
01 1Cefuroxime Sodium
01 1Italy
NDC Package Code : 52946-0905
Start Marketing Date : 2009-12-09
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 Cefuroxime Sodium 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 Cefuroxime Sodium manufacturer or Cefuroxime Sodium supplier for your needs.
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PharmaCompass also assists you with knowing the Cefuroxime Sodium API Price utilized in the formulation of products. Cefuroxime Sodium API Price is not always fixed or binding as the Cefuroxime Sodium Price is obtained through a variety of data sources. The Cefuroxime Sodium Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Cefuroxim Fresenius manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cefuroxim Fresenius, including repackagers and relabelers. The FDA regulates Cefuroxim Fresenius manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cefuroxim Fresenius API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Cefuroxim Fresenius supplier is an individual or a company that provides Cefuroxim Fresenius active pharmaceutical ingredient (API) or Cefuroxim Fresenius finished formulations upon request. The Cefuroxim Fresenius suppliers may include Cefuroxim Fresenius API manufacturers, exporters, distributors and traders.
click here to find a list of Cefuroxim Fresenius 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 Cefuroxim Fresenius as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Cefuroxim Fresenius 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 Cefuroxim Fresenius 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 Cefuroxim Fresenius and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Cefuroxim Fresenius NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Cefuroxim Fresenius suppliers with NDC on PharmaCompass.
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