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01 1Avantor Performance Materials, LLC
02 3Merck KGaA
03 1Nutriplant Industria e Comércio S.A.
04 1Professional Compounding Center of America
05 1SUNLIT FLUO & CHEMICAL CO., L TD. CHUNG-LI FACTORY
06 1Spectrum Laboratory Products, Inc.
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01 1Natrium Fluoride
02 1SODIUM FLUORIDE
03 3Sodium Fluoride
04 3Sodium fluoride
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01 1Brazil
02 1Taiwan
03 5U.S.A
04 1United Kingdom
NDC Package Code : 10106-3689
Start Marketing Date : 2017-12-14
End Marketing Date : 2025-11-08
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 14639-6441
Start Marketing Date : 2010-04-29
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 14639-6441
Start Marketing Date : 2016-06-15
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 14639-6441
Start Marketing Date : 2016-06-15
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (3kg/3kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 82807-002
Start Marketing Date : 2007-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER, FOR SOLUTION (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51927-5225
Start Marketing Date : 2023-11-20
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 49452-6740
Start Marketing Date : 1989-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 62505-001
Start Marketing Date : 2011-01-25
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 Sodium Fluoride 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 Fluoride manufacturer or Sodium Fluoride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Sodium Fluoride manufacturer or Sodium Fluoride supplier.
PharmaCompass also assists you with knowing the Sodium Fluoride API Price utilized in the formulation of products. Sodium Fluoride API Price is not always fixed or binding as the Sodium Fluoride Price is obtained through a variety of data sources. The Sodium Fluoride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Flux manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Flux, including repackagers and relabelers. The FDA regulates Flux manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Flux 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 Flux manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Flux supplier is an individual or a company that provides Flux active pharmaceutical ingredient (API) or Flux finished formulations upon request. The Flux suppliers may include Flux API manufacturers, exporters, distributors and traders.
click here to find a list of Flux 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 Flux as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Flux 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 Flux 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 Flux and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Flux NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Flux suppliers with NDC on PharmaCompass.
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