01 1Eskay Iodine Private Limited
02 1Medisca Inc.
03 1Professional Compounding Centers of America dba PCCA
04 1Spectrum Laboratory Products, Inc.
01 1CLIOQUINOL IODOCHLORHYDROXYQUIN
02 2Clioquinol
03 1Iodochlorhydroxyquinoline
01 1India
02 2U.S.A
03 1United Kingdom
NDC Package Code : 70115-0002
Start Marketing Date : 2017-05-05
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 38779-0032
Start Marketing Date : 2014-07-25
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51927-0096
Start Marketing Date : 2019-02-21
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 49452-2140
Start Marketing Date : 1994-06-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
A Clioquinol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Clioquinol, including repackagers and relabelers. The FDA regulates Clioquinol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Clioquinol 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 Clioquinol manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Clioquinol supplier is an individual or a company that provides Clioquinol active pharmaceutical ingredient (API) or Clioquinol finished formulations upon request. The Clioquinol suppliers may include Clioquinol API manufacturers, exporters, distributors and traders.
click here to find a list of Clioquinol 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 Clioquinol as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Clioquinol 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 Clioquinol 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 Clioquinol and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Clioquinol NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Clioquinol suppliers with NDC on PharmaCompass.
We have 4 companies offering Clioquinol
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