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Data / Drug companies / Nicotinic Acid

Nicotinic Acid drugs: 2 drugs from 31 companies in the FDA NDC directory

Nicotinic Acid is an FDA established pharmacologic class. The FDA National Drug Code Directory lists 72 products in this class from 31 companies, covering 2 drugs by generic name. The main marketing category is other unapproved drugs, and the newest product started marketing on August 6, 2026.

SpecStream is the live web data engine for teams and agents. It reads the National Drug Code Directory that FDA publishes, and this page is that reading. Ask for the companies that make a drug, a class or a dosage form, with their headquarters, website and size added from the web, and new listings and discontinued products arrive in your sheet, CRM, Slack or agent as FDA posts them.

  • 31Companies
  • 72Products
  • 2Drugs by generic name

Drugs in the Nicotinic Acid class

Ranked by number of companies that list the drug.

DrugProducts hereCompanies listing it
Niacin2413
Methyl nicotinate, capsaicin11

Companies with the most products in this class

CompanyProductsMain dosage formsMain marketing categoryNewest product started
PureTek Corporation9tablet; tablet, chewableOther unapproved drugsMay 15, 2025
Bryant Ranch Prepack7tablet, chewable; tabletOther unapproved drugsOctober 1, 2018
Bryant Ranch Prepack4tablet, chewable; tabletOther unapproved drugsOctober 1, 2018
Guna Spa4solution/ drops; pelletUnapproved homeopathic productsDecember 21, 2018
Method Pharmaceuticals, LLC4tablet, chewable; tabletOther unapproved drugsOctober 1, 2018
U.S. Pharmaceutical Corporation4capsule; capsule, liquid filledOther unapproved drugsJune 24, 2009
Amneal Pharmaceuticals LLC3tablet, extended release; tablet, film coated, extended releaseGeneric drugs (ANDA)December 11, 2015
Aurobindo Pharma Limited3tablet, extended releaseGeneric drugs (ANDA)February 1, 2018
Nutritional Specialties, Inc.3spray; liquidUnapproved homeopathic productsJune 5, 2024
Professional Complementary Health Formulas3liquidUnapproved homeopathic productsAugust 15, 1984
Sun Pharmaceutical Industries, Inc.3tablet, film coated, extended releaseGeneric drugs (ANDA)June 27, 2014
Chartwell RX, LLC2tablet, extended releaseGeneric drugs (ANDA)February 16, 2017
Golden State Medical Supply, Inc.2tablet, extended releaseGeneric drugs (ANDA)June 16, 2017
Lannett Company, Inc.2tablet, extended releaseGeneric drugs (ANDA)February 16, 2017
Macleods Pharmaceuticals Limited2tabletGeneric drugs (ANDA)March 3, 2022
Quagen Pharmaceuticals LLC2tablet, extended releaseGeneric drugs (ANDA)August 6, 2026
Advanced Pharmaceutical Services, Inc. Dba Affordable Quality Pharmaceuticals1powderOther unapproved drugsMarch 22, 2024
Apex Energetics Inc.1solution/ dropsUnapproved homeopathic productsAugust 15, 1988
AvPAK1tablet, extended releaseGeneric drugs (ANDA)September 14, 2017
Avondale Pharmaceuticals, LLC1tabletGeneric drugs (ANDA)May 3, 2000
BioActive Nutritional, Inc.1sprayUnapproved homeopathic productsMay 4, 2012
Carwin Pharmaceutical Associates, LLC1capsule, liquid filledOther unapproved drugsJune 1, 2015
Dna Labs, Inc.1solutionUnapproved homeopathic productsJanuary 1, 1990
Emerald Therapeutics, LLC1tabletGeneric drugs (ANDA)May 3, 2000
Exeltis USA, Inc.1capsule, gelatin coatedOther unapproved drugsJune 13, 2011
Key 2 Health, Inc.1creamOver the counter monograph drugsFebruary 11, 2011
Lupin Pharmaceuticals, Inc.1tablet, extended releaseGeneric drugs (ANDA)March 20, 2014
Oncora Pharma, LLC1tablet, chewableOther unapproved drugsApril 7, 2026
Redmont Pharmaceuticals, LLC1tabletGeneric drugs (ANDA)May 3, 2000
Remedyrepack Inc.1tabletOther unapproved drugsNovember 5, 2022
Strand Health Group1patchOver the counter monograph drugsJune 29, 2023

Dosage forms

Dosage formProductsShare
Tablet, chewable1723.6%
Tablet, extended release1520.8%
Tablet1419.4%
Liquid45.6%
Solution/ drops45.6%
Tablet, film coated, extended release45.6%
Capsule34.2%
Spray34.2%
Capsule, liquid filled22.8%
Capsule, gelatin coated11.4%
Powder11.4%
Pellet11.4%

Updated November 6, 2026. Read from US Food and Drug Administration, National Drug Code Directory (openFDA). CC0 1.0 public domain dedication (openFDA). Counts are products in the FDA National Drug Code Directory on November 6, 2026: 138,262 products in commercial distribution, meaning without a marketing end date in the past. A company is a labeler code; one company can hold several codes, and the directory carries no address. Inclusion in the directory is not FDA approval, and the marketing category says under which kind of application or rule a product is sold. This page uses openFDA data and is not endorsed or certified by FDA. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.