01 1Curia New York, Inc.
02 1Honour Lab Limited
03 1Sionc Pharmaceutical Private Limited
04 1Vasudha Pharma Chem Limited
01 3Diatrizoate Sodium
02 1diatrizoate sodium
01 3India
02 1U.S.A
NDC Package Code : 65392-1701
Start Marketing Date : 1954-11-26
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (65kg/65kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 69037-0052
Start Marketing Date : 1982-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 76055-0014
Start Marketing Date : 2019-12-31
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 66577-032
Start Marketing Date : 2018-12-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Diatrizoate Sodium manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Diatrizoate Sodium, including repackagers and relabelers. The FDA regulates Diatrizoate Sodium manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Diatrizoate Sodium 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 Diatrizoate Sodium manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Diatrizoate Sodium supplier is an individual or a company that provides Diatrizoate Sodium active pharmaceutical ingredient (API) or Diatrizoate Sodium finished formulations upon request. The Diatrizoate Sodium suppliers may include Diatrizoate Sodium API manufacturers, exporters, distributors and traders.
click here to find a list of Diatrizoate Sodium 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 Diatrizoate Sodium as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Diatrizoate Sodium 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 Diatrizoate Sodium 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 Diatrizoate Sodium and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Diatrizoate Sodium NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Diatrizoate Sodium suppliers with NDC on PharmaCompass.
We have 4 companies offering Diatrizoate Sodium
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