01 1BK Giulini GmbH
02 1Elementis Pharma Gmbh
03 1Nutriplant Industria Comercio S.A.
04 1Srikem laboratories Pvt. Ltd.
01 1SODIUM MONOFLUOROPHOSPHATE
02 1Sodium Monofluoro Phosphate
03 2Sodium Monofluorophosphate
01 1Brazil
02 2Germany
03 1India
NDC Package Code : 73608-000
Start Marketing Date : 2020-04-25
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 55603-240
Start Marketing Date : 2011-03-28
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 82807-003
Start Marketing Date : 2023-03-20
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER, FOR SOLUTION (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 13746-117
Start Marketing Date : 2016-04-16
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Fluorophosphate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Fluorophosphate, including repackagers and relabelers. The FDA regulates Fluorophosphate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Fluorophosphate API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Fluorophosphate supplier is an individual or a company that provides Fluorophosphate active pharmaceutical ingredient (API) or Fluorophosphate finished formulations upon request. The Fluorophosphate suppliers may include Fluorophosphate API manufacturers, exporters, distributors and traders.
click here to find a list of Fluorophosphate 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 Fluorophosphate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Fluorophosphate 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 Fluorophosphate 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 Fluorophosphate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Fluorophosphate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Fluorophosphate suppliers with NDC on PharmaCompass.
We have 4 companies offering Fluorophosphate
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