01 1Global Calcium Private Limited
02 1Harman Finochem Limited
03 1QUALITY CHEMICALS S.L.
01 2Potassium Acetate
02 1Potassium acetate
01 2India
02 1Spain
NDC Package Code : 64162-0098
Start Marketing Date : 2024-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 66064-1037
Start Marketing Date : 2021-07-01
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 56141-006
Start Marketing Date : 2023-12-13
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 Potassium 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 Potassium Acetate manufacturer or Potassium Acetate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Potassium Acetate manufacturer or Potassium Acetate supplier.
PharmaCompass also assists you with knowing the Potassium Acetate API Price utilized in the formulation of products. Potassium Acetate API Price is not always fixed or binding as the Potassium Acetate Price is obtained through a variety of data sources. The Potassium Acetate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A E261 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of E261, including repackagers and relabelers. The FDA regulates E261 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. E261 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 E261 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A E261 supplier is an individual or a company that provides E261 active pharmaceutical ingredient (API) or E261 finished formulations upon request. The E261 suppliers may include E261 API manufacturers, exporters, distributors and traders.
click here to find a list of E261 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 E261 as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for E261 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 E261 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 E261 and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a E261 NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of E261 suppliers with NDC on PharmaCompass.
We have 3 companies offering E261
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