01 1DSM Nutritional Products LLC
02 1Fagron Inc
03 1Medisca Inc.
04 1Second Pharma Co., Ltd.
01 1NIACINAMIDE
02 3Niacinamide
01 1China
02 2Netherlands
03 1U.S.A
NDC Package Code : 51552-0771
Start Marketing Date : 1998-04-01
End Marketing Date : 2026-06-27
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 38779-3303
Start Marketing Date : 2023-11-23
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 63238-3600
Start Marketing Date : 2018-03-09
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 57845-1007
Start Marketing Date : 2021-03-17
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
A Niacinamide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Niacinamide, including repackagers and relabelers. The FDA regulates Niacinamide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Niacinamide 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 Niacinamide manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Niacinamide supplier is an individual or a company that provides Niacinamide active pharmaceutical ingredient (API) or Niacinamide finished formulations upon request. The Niacinamide suppliers may include Niacinamide API manufacturers, exporters, distributors and traders.
click here to find a list of Niacinamide 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 Niacinamide as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Niacinamide 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 Niacinamide 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 Niacinamide and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Niacinamide NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Niacinamide suppliers with NDC on PharmaCompass.
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