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Data / Drug companies / Acetaminophen, aspirin and caffeine

Acetaminophen, aspirin and caffeine: 26 companies and 29 products in the FDA NDC directory

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

Acetaminophen, aspirin and caffeine is listed in the FDA National Drug Code Directory by 26 companies, with 29 products in commercial distribution. 15 of the products (51.7%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are tablet, film coated; tablet; tablet, coated, and the newest product started marketing on March 17, 2026.

The request: Get every company that lists acetaminophen, aspirin and caffeine 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
26
Products
29
Generic (ANDA) products
15 (51.7%)
Application numbers
4
Routes
Oral
Brand names
Headache Relief Extra Strength, Migraine Relief, Acetaminophen Aspirin and Caffeine, Extra Strength Pain Reliever, Extra Pain Relief, Publix Super Markets Inc, Amazon Basic Care Migraine Relief, Pain Reliever Extra Strength
openFDA record search
api.fda.gov

Companies that list acetaminophen, aspirin and caffeine

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

CompanyProductsMain dosage formsMain marketing categoryNewest product started
Aurohealth LLC2tablet, film coatedGeneric drugs (ANDA)June 23, 2022
Safeway2tablet; tablet, film coatedGeneric drugs (ANDA)August 11, 2023
Salado Sales, Inc.2tablet, film coatedOver the counter monograph drugsMarch 13, 2008
Aaa Pharmaceutical, Inc.1tabletGeneric drugs (ANDA)May 3, 2023
Allegiant Health1tablet, film coatedOver the counter monograph drugsFebruary 15, 2010
Amazon.com Services LLC1tablet, film coatedGeneric drugs (ANDA)May 15, 2024
CVS Pharmacy1tablet, film coatedOver the counter monograph drugsMarch 13, 2008
Chain Drug Marketing Association1tablet, film coatedOver the counter monograph drugsNovember 17, 1992
Chain Drug Marketing Association, Inc.1tabletGeneric drugs (ANDA)May 1, 2024
Discount Drug Mart1tabletGeneric drugs (ANDA)January 11, 2024
Family Dollar (family Wellness)1tabletGeneric drugs (ANDA)September 1, 2023
Fsa Store Inc.1tabletGeneric drugs (ANDA)January 11, 2023
Geri-Care Pharmaceuticals, Corp1tablet, film coatedOver the counter monograph drugsFebruary 1, 2020
Granules India Limited1tabletGeneric drugs (ANDA)April 15, 2021
Grocery Outlet, Inc.1tablet, film coatedOver the counter monograph drugsMarch 17, 2026
Harris Teeter1tabletGeneric drugs (ANDA)August 30, 2023
Kroger Company1tablet, coatedOver the counter monograph drugsApril 10, 2021
Proficient Rx LP1tablet, film coatedOver the counter monograph drugsFebruary 1, 2020
Publix Super Markets Inc1tabletGeneric drugs (ANDA)February 23, 2024
Rising Pharma Holdings, Inc.1tabletOver the counter monograph drugsJuly 9, 2025
Rite Aid Corporation1tablet, film coatedOver the counter monograph drugsNovember 17, 1992
Safrel Pharmaceuticals, LLC.1tabletGeneric drugs (ANDA)April 15, 2021
Time Cap Laboratories, Inc1tablet, film coatedOver the counter monograph drugsNovember 1, 2013
Valu Merchandisers Company1tablet, film coatedOver the counter monograph drugsNovember 17, 1992
Wal-Mart Stores Inc1tablet, film coatedOver the counter monograph drugsMarch 13, 2008
Walmart Inc.1tablet, film coatedGeneric drugs (ANDA)February 28, 2024

Dosage forms

Dosage formProductsShare
Tablet, film coated1758.6%
Tablet1137.9%
Tablet, coated13.4%

Marketing categories

Marketing categoryProductsShare
Generic drugs (ANDA)1551.7%
Over the counter monograph drugs1448.3%

Pharmacologic classes

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.