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Data / Drug companies / Acetaminophen 500 mg

Acetaminophen 500 mg: 6 companies and 6 products in the FDA NDC directory

Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).

Acetaminophen 500 mg is listed in the FDA National Drug Code Directory by 6 companies, with 6 products in commercial distribution. 0 of the products (0.0%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are tablet, film coated; tablet; capsule, liquid filled, and the newest product started marketing on August 4, 2026.

The request: Get every company that lists acetaminophen 500 mg in the FDA NDC directory, with headquarters, website and number of employees. $10 of work on sign-up, no card.

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Companies listing it
6
Products
6
Generic (ANDA) products
0 (0.0%)
Application numbers
1
Routes
Oral
Brand names
Medique at Home Apap Extra Strength, Crane Safety XS Non-Aspirin, Extra Strength Pain Reliever, Pain Relief Extra Strength, Extra Strength Pain Reliever Mini Softgels
openFDA record search
api.fda.gov

Companies that list acetaminophen 500 mg

Ranked by number of products. Finished drugs in commercial distribution.

CompanyProductsMain dosage formsMain marketing categoryNewest product started
Allegiant Health1tabletOver the counter monograph drugsDecember 17, 2014
Lil' Drug Store Products, Inc.1tabletOver the counter monograph drugsJanuary 17, 2017
Shield Pharmaceuticals Corp1capsule, liquid filledOver the counter monograph drugsAugust 4, 2026
Sportpharm LLC1tablet, film coatedOver the counter monograph drugsFebruary 1, 2021
Thompson1tablet, film coatedOver the counter monograph drugsJanuary 17, 2020
Unifirst First Aid Corporation1tablet, film coatedOver the counter monograph drugsFebruary 1, 2021

Dosage forms

Dosage formProductsShare
Tablet, film coated350%
Tablet233.3%
Capsule, liquid filled116.7%

Marketing categories

Marketing categoryProductsShare
Over the counter monograph drugs6100%

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.