01 1NANHAI BEISHA PHARMACEUTICAL CO., LTD.
01 1SULFAQUINOXALINE
01 1China
NDC Package Code : 63422-704
Start Marketing Date : 2016-06-21
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 Sulfaquinoxaline 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 Sulfaquinoxaline manufacturer or Sulfaquinoxaline supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Sulfaquinoxaline manufacturer or Sulfaquinoxaline supplier.
PharmaCompass also assists you with knowing the Sulfaquinoxaline API Price utilized in the formulation of products. Sulfaquinoxaline API Price is not always fixed or binding as the Sulfaquinoxaline Price is obtained through a variety of data sources. The Sulfaquinoxaline Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Sulfacox manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sulfacox, including repackagers and relabelers. The FDA regulates Sulfacox manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sulfacox 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 Sulfacox supplier is an individual or a company that provides Sulfacox active pharmaceutical ingredient (API) or Sulfacox finished formulations upon request. The Sulfacox suppliers may include Sulfacox API manufacturers, exporters, distributors and traders.
click here to find a list of Sulfacox 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 Sulfacox as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Sulfacox 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 Sulfacox 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 Sulfacox and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Sulfacox NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Sulfacox suppliers with NDC on PharmaCompass.
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