01 1Ganesh Benzoplast Limited
02 1MSN Life Sciences Private Limited
03 1Sigma-Aldrich Ireland Ltd.
01 1SODIUM BENZOATE
02 2Sodium Benzoate
01 1India
02 1U.S.A
03 1Blank
NDC Package Code : 69766-028
Start Marketing Date : 2016-12-28
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 54154-024
Start Marketing Date : 2019-02-28
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 84364-000
Start Marketing Date : 2024-10-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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A Sodium Benzoate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sodium Benzoate, including repackagers and relabelers. The FDA regulates Sodium Benzoate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sodium Benzoate 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 Sodium Benzoate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Sodium Benzoate supplier is an individual or a company that provides Sodium Benzoate active pharmaceutical ingredient (API) or Sodium Benzoate finished formulations upon request. The Sodium Benzoate suppliers may include Sodium Benzoate API manufacturers, exporters, distributors and traders.
click here to find a list of Sodium Benzoate 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 Sodium Benzoate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Sodium Benzoate 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 Sodium Benzoate 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 Sodium Benzoate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Sodium Benzoate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Sodium Benzoate suppliers with NDC on PharmaCompass.
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