01 1Jost Chemical Co.
01 1Sodium Caprylate
01 1U.S.A
NDC Package Code : 55570-401
Start Marketing Date : 2020-01-22
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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A Prifac 2901 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Prifac 2901, including repackagers and relabelers. The FDA regulates Prifac 2901 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Prifac 2901 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 Prifac 2901 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Prifac 2901 supplier is an individual or a company that provides Prifac 2901 active pharmaceutical ingredient (API) or Prifac 2901 finished formulations upon request. The Prifac 2901 suppliers may include Prifac 2901 API manufacturers, exporters, distributors and traders.
click here to find a list of Prifac 2901 suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 Prifac 2901 as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Prifac 2901 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 Prifac 2901 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 Prifac 2901 and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Prifac 2901 NDC to their finished compounded human drug products, they may choose to do so.
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