01 1Siegfried Evionnaz SA
01 1Choline Salicylate
01 1Switzerland
NDC Package Code : 17381-251
Start Marketing Date : 2010-04-08
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 Choline Salicylate 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 Choline Salicylate manufacturer or Choline Salicylate supplier for your needs.
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PharmaCompass also assists you with knowing the Choline Salicylate API Price utilized in the formulation of products. Choline Salicylate API Price is not always fixed or binding as the Choline Salicylate Price is obtained through a variety of data sources. The Choline Salicylate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Mundisal manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Mundisal, including repackagers and relabelers. The FDA regulates Mundisal manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Mundisal 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 Mundisal manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Mundisal supplier is an individual or a company that provides Mundisal active pharmaceutical ingredient (API) or Mundisal finished formulations upon request. The Mundisal suppliers may include Mundisal API manufacturers, exporters, distributors and traders.
click here to find a list of Mundisal 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 Mundisal as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Mundisal 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 Mundisal 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 Mundisal and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Mundisal NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Mundisal suppliers with NDC on PharmaCompass.
