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Data / Drug companies / Acetaminophen and diphenhydramine hydrochloride

Acetaminophen and diphenhydramine hydrochloride: 29 companies and 37 products in the FDA NDC directory

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

Acetaminophen and diphenhydramine hydrochloride is listed in the FDA National Drug Code Directory by 29 companies, with 37 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, coated; tablet; tablet, film coated, and the newest product started marketing on June 20, 2026.

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Companies listing it
29
Products
37
Generic (ANDA) products
0 (0.0%)
Application numbers
2
Routes
Oral
Brand names
Pain Relief PM Extra Strength, Acetaminophen PM, Pain Relief PM, Tylenol PM Extra Strength, Extra Strength Pain Reliever PM, Tylenol PM Extra Strength, CVP Health, Acetaminophen PM Extra Strength, Chloraseptic Nighttime Sore Throat Hot Relief
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Companies that list acetaminophen and diphenhydramine hydrochloride

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

CompanyProductsMain dosage formsMain marketing categoryNewest product started
Lil' Drug Store Products, Inc.3tablet, film coatedOver the counter monograph drugsMay 6, 2022
Harris Teeter2tablet, coatedOver the counter monograph drugsJune 6, 2014
Kenvue Brands LLC2tablet, film coated; solutionOver the counter monograph drugsJune 25, 2018
Kroger Company2tabletOver the counter monograph drugsMay 1, 2021
Marc Glassman, Inc.2tablet, coatedOver the counter monograph drugsOctober 5, 2022
Safeway2tablet; tablet, coatedOver the counter monograph drugsNovember 18, 2023
Walmart Inc.2tabletOver the counter monograph drugsJune 28, 2024
Aaa Pharmaceutical, Inc.1tablet, coatedOver the counter monograph drugsOctober 1, 2012
Amerifoods Trading Company1tablet, coatedOver the counter monograph drugsOctober 30, 2023
Aurohealth LLC1tabletOver the counter monograph drugsJanuary 5, 2021
Bi-Mart1tabletOver the counter monograph drugsFebruary 1, 2025
Chain Drug Marketing Association1tablet, coatedOver the counter monograph drugsNovember 8, 2007
Chain Drug Marketing Association, Inc.1tablet, coatedOver the counter monograph drugsApril 29, 2024
Chattem, Inc.1tablet, film coatedOver the counter monograph drugsDecember 1, 2009
Fsa Store Inc.1tablet, coatedOver the counter monograph drugsMay 2, 2023
Grocery Outlet, Inc.1tablet, coatedOver the counter monograph drugsFebruary 18, 2026
H E B1tablet, coatedOver the counter monograph drugsFebruary 1, 2013
Haleon US Holdings LLC1solutionOver the counter monograph drugsJune 15, 2020
HyVee Inc1tablet, coatedOver the counter monograph drugsOctober 22, 2025
Navajo Manufacturing Company Inc.1tablet, film coatedOver the counter monograph drugsMarch 11, 2025
Perrigo Direct, Inc1tablet, coatedOver the counter monograph drugsAugust 1, 2017
Prestige Brands Holdings, Inc.1powder, for solutionOver the counter monograph drugsJune 20, 2026
Retail Business Services, LLC1tablet, coatedOver the counter monograph drugsMarch 1, 2024
Select Consumer Group1tablet, film coatedOver the counter monograph drugsJuly 11, 2016
Topco Associates LLC1tablet, coatedOver the counter monograph drugsNovember 30, 2012
United Natural Foods, Inc. DBA Unfi1tablet, coatedOver the counter monograph drugsSeptember 1, 2014
Valu Merchandisers Company1tablet, coatedOver the counter monograph drugsFebruary 1, 2010
Walgreen Company1tabletOver the counter monograph drugsApril 13, 2023
WinCo Foods, LLC1tablet, coatedOver the counter monograph drugsDecember 15, 2014

Dosage forms

Dosage formProductsShare
Tablet, coated1951.4%
Tablet821.6%
Tablet, film coated718.9%
Solution25.4%
Powder, for solution12.7%

Marketing categories

Marketing categoryProductsShare
Over the counter monograph drugs37100%

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.