01 1JUSTESA IMAGEN S.A.U.
02 1Vasudha Pharma Chem Limited
01 1DIATRIZOIC ACID DIHYDRATE
02 1Diatrizoic Acid Dihydrate
01 1India
02 1Spain
NDC Package Code : 52134-0500
Start Marketing Date : 2009-08-11
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 66577-030
Start Marketing Date : 2018-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Diatrizoic Acid manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Diatrizoic Acid, including repackagers and relabelers. The FDA regulates Diatrizoic Acid manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Diatrizoic Acid 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 Diatrizoic Acid manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Diatrizoic Acid supplier is an individual or a company that provides Diatrizoic Acid active pharmaceutical ingredient (API) or Diatrizoic Acid finished formulations upon request. The Diatrizoic Acid suppliers may include Diatrizoic Acid API manufacturers, exporters, distributors and traders.
click here to find a list of Diatrizoic Acid 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 Diatrizoic Acid as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Diatrizoic Acid 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 Diatrizoic Acid 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 Diatrizoic Acid and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Diatrizoic Acid NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Diatrizoic Acid suppliers with NDC on PharmaCompass.
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