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Data / Drug companies / Diphenhydramine citrate, ibuprofen

Diphenhydramine citrate, ibuprofen: 19 companies and 20 products in the FDA NDC directory

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

Diphenhydramine citrate, ibuprofen is listed in the FDA National Drug Code Directory by 19 companies, with 20 products in commercial distribution. 19 of the products (95.0%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are tablet, film coated; tablet, coated, and the newest product started marketing on December 29, 2025.

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Companies listing it
19
Products
20
Generic (ANDA) products
19 (95.0%)
Application numbers
3
Routes
Oral
Brand names
Ibuprofen PM, Ibuprofen PM, Advil PM, Foster and Thrive Ibuprofen PM, Equaline Ibuprofen PM, Good Sense Ibuprofen PM, Exchange Select Ibuprofen PM, Ibuprofen PM
openFDA record search
api.fda.gov

Companies that list diphenhydramine citrate, ibuprofen

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

CompanyProductsMain dosage formsMain marketing categoryNewest product started
Safeway2tablet, coated; tablet, film coatedGeneric drugs (ANDA)December 29, 2025
Amazon.com Services LLC1tablet, film coatedGeneric drugs (ANDA)April 30, 2021
Amerisource Bergen1tablet, film coatedGeneric drugs (ANDA)April 1, 2022
Army and Air Force Exchange Service1tablet, film coatedGeneric drugs (ANDA)August 28, 2015
Cardinal Health 110, LLC. DBA Leader1tablet, film coatedGeneric drugs (ANDA)November 23, 2016
Family Dollar (family Wellness)1tablet, coatedGeneric drugs (ANDA)March 1, 2024
H E B1tablet, film coatedGeneric drugs (ANDA)April 5, 2018
HyVee Inc1tablet, film coatedGeneric drugs (ANDA)March 2, 2009
Kroger Company1tablet, film coatedGeneric drugs (ANDA)April 6, 2009
L. Perrigo Company1tablet, film coatedGeneric drugs (ANDA)March 5, 2009
Meijer Distribution Inc1tablet, film coatedGeneric drugs (ANDA)April 8, 2009
Navajo Manufacturing Company Inc.1tablet, coatedNew drug applications (NDA)September 16, 2016
Publix Super Markets Inc1tablet, film coatedGeneric drugs (ANDA)September 15, 2011
Strategic Sourcing Services LLC1tablet, film coatedGeneric drugs (ANDA)November 1, 2023
United Natural Foods, Inc. DBA Unfi1tablet, film coatedGeneric drugs (ANDA)March 2, 2009
WR Group, Inc.1tablet, coatedGeneric drugs (ANDA)February 28, 2025
Wal-Mart Stores Inc1tablet, film coatedGeneric drugs (ANDA)April 15, 2009
Walgreen Company1tablet, film coatedGeneric drugs (ANDA)February 19, 2009
Walmart Inc.1tablet, coatedGeneric drugs (ANDA)June 8, 2024

Dosage forms

Dosage formProductsShare
Tablet, film coated1575%
Tablet, coated525%

Marketing categories

Marketing categoryProductsShare
Generic drugs (ANDA)1995%
New drug applications (NDA)15%

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.