01 1Arkema, Inc
02 1Cambrex Karlskoga AB
03 1Corden Pharma Bergamo S.p.A.
04 7Nouryon Chemicals, S.A. de C.V.
05 1Professional Compounding Centers of America dba PCCA
06 1Spectrum Laboratory Products, Inc.
01 8BENZOYL PEROXIDE
02 1Benzoyl Peroxide
03 1Benzoyl Peroxide Powder Water Wet
04 1Benzoyl Peroxide, Hydrous
05 1Benzoyl peroxide, hydrous
01 1France
02 1Italy
03 7Netherlands
04 2U.S.A
05 1United Kingdom
NDC Package Code : 17129-002
Start Marketing Date : 1960-10-10
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (100kg/100kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 12651-115
Start Marketing Date : 2000-12-27
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 49964-0027
Start Marketing Date : 2009-09-17
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 67645-342
Start Marketing Date : 1997-11-03
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (78kg/100kg)
Marketing Category : DRUG FOR FURTHER PROCESSING
NDC Package Code : 67645-340
Start Marketing Date : 1997-11-03
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (75kg/100kg)
Marketing Category : DRUG FOR FURTHER PROCESSING
NDC Package Code : 67645-341
Start Marketing Date : 1997-11-03
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (78kg/100kg)
Marketing Category : DRUG FOR FURTHER PROCESSING
NDC Package Code : 67645-344
Start Marketing Date : 1997-11-03
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (75kg/100kg)
Marketing Category : DRUG FOR FURTHER PROCESSING
NDC Package Code : 67645-343
Start Marketing Date : 1997-11-03
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (75kg/100kg)
Marketing Category : DRUG FOR FURTHER PROCESSING
NDC Package Code : 51927-3085
Start Marketing Date : 2002-07-19
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (100kg/100kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 49452-1010
Start Marketing Date : 1996-07-30
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (75kg/100kg)
Marketing Category : DRUG FOR FURTHER PROCESSING
A Benzoyl Peroxide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Benzoyl Peroxide, including repackagers and relabelers. The FDA regulates Benzoyl Peroxide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Benzoyl Peroxide 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 Benzoyl Peroxide manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Benzoyl Peroxide supplier is an individual or a company that provides Benzoyl Peroxide active pharmaceutical ingredient (API) or Benzoyl Peroxide finished formulations upon request. The Benzoyl Peroxide suppliers may include Benzoyl Peroxide API manufacturers, exporters, distributors and traders.
click here to find a list of Benzoyl Peroxide 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 Benzoyl Peroxide as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Benzoyl Peroxide 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 Benzoyl Peroxide 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 Benzoyl Peroxide and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Benzoyl Peroxide NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Benzoyl Peroxide suppliers with NDC on PharmaCompass.
We have 6 companies offering Benzoyl Peroxide
Get in contact with the supplier of your choice:
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