01 2Macco Organiques Inc
02 1Spectrum Laboratory Products, Inc.
01 2SODIUM ACETATE
02 1Sodium Acetate
01 2Canada
02 1U.S.A
NDC Package Code : 55897-003
Start Marketing Date : 2021-04-15
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 55897-001
Start Marketing Date : 2012-02-17
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (100kg/100kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 49452-6550
Start Marketing Date : 1986-02-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Sodium Acetate 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 Sodium Acetate manufacturer or Sodium Acetate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Sodium Acetate manufacturer or Sodium Acetate supplier.
PharmaCompass also assists you with knowing the Sodium Acetate API Price utilized in the formulation of products. Sodium Acetate API Price is not always fixed or binding as the Sodium Acetate Price is obtained through a variety of data sources. The Sodium Acetate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A E262 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of E262, including repackagers and relabelers. The FDA regulates E262 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. E262 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 E262 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A E262 supplier is an individual or a company that provides E262 active pharmaceutical ingredient (API) or E262 finished formulations upon request. The E262 suppliers may include E262 API manufacturers, exporters, distributors and traders.
click here to find a list of E262 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 E262 as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for E262 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 E262 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 E262 and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a E262 NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of E262 suppliers with NDC on PharmaCompass.
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