01 1AARTI DRUGS LTD
02 1Divi's Laboratories Limited
03 1Jubilant Pharmova Limited
04 1Vertellus LLC
01 3Niacin
02 1niacin
01 3India
02 1Blank
NDC Package Code : 62704-0027
Start Marketing Date : 1993-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 62331-016
Start Marketing Date : 2004-07-20
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65372-1194
Start Marketing Date : 2017-03-28
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 25441-0095
Start Marketing Date : 2021-11-30
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
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A Niaspan manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Niaspan, including repackagers and relabelers. The FDA regulates Niaspan manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Niaspan 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 Niaspan manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Niaspan supplier is an individual or a company that provides Niaspan active pharmaceutical ingredient (API) or Niaspan finished formulations upon request. The Niaspan suppliers may include Niaspan API manufacturers, exporters, distributors and traders.
click here to find a list of Niaspan 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 Niaspan as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Niaspan 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 Niaspan 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 Niaspan and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Niaspan NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Niaspan suppliers with NDC on PharmaCompass.
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