01 1Trifarma S.p.A
01 1Prochlorperazine
01 1Italy
NDC Package Code : 46204-0007
Start Marketing Date : 2012-05-04
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 Prochlorperazine 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 Prochlorperazine manufacturer or Prochlorperazine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Prochlorperazine manufacturer or Prochlorperazine supplier.
PharmaCompass also assists you with knowing the Prochlorperazine API Price utilized in the formulation of products. Prochlorperazine API Price is not always fixed or binding as the Prochlorperazine Price is obtained through a variety of data sources. The Prochlorperazine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Eskatrol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Eskatrol, including repackagers and relabelers. The FDA regulates Eskatrol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Eskatrol 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 Eskatrol manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Eskatrol supplier is an individual or a company that provides Eskatrol active pharmaceutical ingredient (API) or Eskatrol finished formulations upon request. The Eskatrol suppliers may include Eskatrol API manufacturers, exporters, distributors and traders.
click here to find a list of Eskatrol 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 Eskatrol as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Eskatrol 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 Eskatrol 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 Eskatrol and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Eskatrol NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Eskatrol suppliers with NDC on PharmaCompass.
