01 1APICORE PHARMACEUTICALS PRIVATE LIMITED
02 1Chongqing Huapont Pharmaceutical Co Limited
03 1Corden Pharma Bergamo S.p.A.
04 1Matrix Pharmacorp Private Limited
05 1Solara Active Pharma Sciences Limited
01 1DISULFIRAM
02 2Disulfiram
03 1Disulfiram Powdered
04 1Tetrandrine
01 1China
02 2India
03 1Italy
04 1Blank
NDC Package Code : 42973-137
Start Marketing Date : 2008-11-01
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 48943-0015
Start Marketing Date : 2011-03-10
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 49964-0032
Start Marketing Date : 2009-09-24
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 72643-028
Start Marketing Date : 2022-03-07
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 84206-0115
Start Marketing Date : 2025-08-14
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Disulfiram API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Disulfiram manufacturer or Disulfiram supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Disulfiram manufacturer or Disulfiram supplier.
A Disulfiram manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Disulfiram, including repackagers and relabelers. The FDA regulates Disulfiram manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Disulfiram 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 Disulfiram manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Disulfiram supplier is an individual or a company that provides Disulfiram active pharmaceutical ingredient (API) or Disulfiram finished formulations upon request. The Disulfiram suppliers may include Disulfiram API manufacturers, exporters, distributors and traders.
click here to find a list of Disulfiram suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 Disulfiram as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Disulfiram 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 Disulfiram 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 Disulfiram and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Disulfiram NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Disulfiram suppliers with NDC on PharmaCompass.
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