01 2Derivados Quimicos
02 1PROCOS SpA
01 2Clofazimine
02 1Clofazimine micronized
01 1Italy
02 2Spain
NDC Package Code : 59349-0030
Start Marketing Date : 2023-03-03
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 59349-0031
Start Marketing Date : 2023-03-02
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 46016-2030
Start Marketing Date : 2018-11-26
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT
A Clofazimine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Clofazimine, including repackagers and relabelers. The FDA regulates Clofazimine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Clofazimine 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 Clofazimine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Clofazimine supplier is an individual or a company that provides Clofazimine active pharmaceutical ingredient (API) or Clofazimine finished formulations upon request. The Clofazimine suppliers may include Clofazimine API manufacturers, exporters, distributors and traders.
click here to find a list of Clofazimine 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 Clofazimine as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Clofazimine 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 Clofazimine 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 Clofazimine and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Clofazimine NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Clofazimine suppliers with NDC on PharmaCompass.
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