Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.
01 2Biophore India Pharmaceuticals Pvt. Ltd
02 2Jost Chemical Co.
03 3Merck KGaA
04 1Spectrum Laboratory Products, Inc.
01 3Potassium Phosphate Dibasic
02 2Potassium Phosphate Monobasic
03 3di-Potassium hydrogen phosphate
01 2India
02 6U.S.A
Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.
POTASSIUM PHOSPHATE, MONOBASIC
NDC Package Code : 73435-032
Start Marketing Date : 2023-10-31
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (60kg/60kg)
Marketing Category : BULK INGREDIENT
Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.
NDC Package Code : 73435-033
Start Marketing Date : 2023-10-31
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (60kg/60kg)
Marketing Category : BULK INGREDIENT
POTASSIUM PHOSPHATE, MONOBASIC
NDC Package Code : 55570-390
Start Marketing Date : 2007-04-11
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 55570-380
Start Marketing Date : 2007-01-05
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 14639-9828
Start Marketing Date : 2014-07-07
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 14639-9828
Start Marketing Date : 2010-12-17
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (12kg/12kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 14639-9828
Start Marketing Date : 2015-10-07
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 49452-5921
Start Marketing Date : 1995-08-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
A Dibasic potassium phosphate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dibasic potassium phosphate, including repackagers and relabelers. The FDA regulates Dibasic potassium phosphate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dibasic potassium phosphate 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 Dibasic potassium phosphate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Dibasic potassium phosphate supplier is an individual or a company that provides Dibasic potassium phosphate active pharmaceutical ingredient (API) or Dibasic potassium phosphate finished formulations upon request. The Dibasic potassium phosphate suppliers may include Dibasic potassium phosphate API manufacturers, exporters, distributors and traders.
click here to find a list of Dibasic potassium phosphate 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 Dibasic potassium phosphate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Dibasic potassium phosphate 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 Dibasic potassium phosphate 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 Dibasic potassium phosphate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Dibasic potassium phosphate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Dibasic potassium phosphate suppliers with NDC on PharmaCompass.
We have 4 companies offering Dibasic potassium phosphate
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