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Data / Drug companies / Doxylamine succinate

Doxylamine succinate: 39 companies and 53 products in the FDA NDC directory

Doxylamine succinate is listed in the FDA National Drug Code Directory by 39 companies, with 53 products in commercial distribution. 46 of the products (86.8%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are tablet; liquid; tablet, coated, and the newest product started marketing on August 27, 2026.

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Companies listing it
39
Products
53
Generic (ANDA) products
46 (86.8%)
Application numbers
4
Routes
Oral
Brand names
Sleep Aid, Nighttime Sleep Aid, Sleep Aid, Unisom SleepTabs, Good Sense Sleep Aid Ultra, Vicks ZzzQuil Ultra, Sleep Aid, Night Time Sleep Aid
openFDA record search
api.fda.gov

Companies that list doxylamine succinate

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

CompanyProductsMain dosage formsMain marketing categoryNewest product started
L. Perrigo Company3tablet; tablet, coatedGeneric drugs (ANDA)February 27, 2025
The Procter & Gamble Manufacturing Company3liquid; capsule, liquid filledOver the counter monograph drugsJuly 1, 2026
Walgreen Company3tablet; liquidGeneric drugs (ANDA)February 9, 2026
Amazon.com Services LLC2tabletGeneric drugs (ANDA)August 27, 2026
Chattem, Inc.2tabletGeneric drugs (ANDA)March 16, 2026
Kroger Company2tabletGeneric drugs (ANDA)September 9, 2023
L.N.K. International, Inc.2tabletGeneric drugs (ANDA)July 23, 2019
Lil' Drug Store Products, Inc.2tabletOver the counter monograph drugsJanuary 26, 2024
Meijer Distribution Inc2tabletGeneric drugs (ANDA)May 6, 2019
Rite Aid Corporation2tabletGeneric drugs (ANDA)July 19, 2023
Topco Associates LLC2tablet, coated; tabletGeneric drugs (ANDA)March 26, 2025
Advanced Rx LLC1tabletGeneric drugs (ANDA)August 27, 2004
American Sales Company1tabletGeneric drugs (ANDA)May 6, 2016
Amerisource Bergen1tabletGeneric drugs (ANDA)June 7, 2024
Army and Air Force Exchange Service1tabletGeneric drugs (ANDA)April 1, 2019
Belmora LLC1tabletGeneric drugs (ANDA)October 31, 2019
Bi-Mart1tabletGeneric drugs (ANDA)June 1, 2025
Bjwc1tabletGeneric drugs (ANDA)August 6, 2018
CVS Pharmacy1tabletGeneric drugs (ANDA)July 23, 1997
CVS Pharmacy1tabletGeneric drugs (ANDA)July 20, 2019
CVS Woonsocket Prescription Center, Incorporated1tabletGeneric drugs (ANDA)June 25, 2025
Cardinal Health 110, LLC. DBA Leader1tabletGeneric drugs (ANDA)July 23, 2020
Costco Wholesale Company1tabletGeneric drugs (ANDA)May 3, 2019
Dolgencorp, Inc. (dollar General & Rexall)1tabletGeneric drugs (ANDA)May 17, 2023
Grocery Outlet, Inc.1tabletGeneric drugs (ANDA)March 18, 2026
H E B1tabletGeneric drugs (ANDA)July 15, 2019
HyVee Inc1tabletGeneric drugs (ANDA)December 4, 2014
Meijer, Inc.1tabletGeneric drugs (ANDA)July 29, 2022
Publix Super Markets Inc1tabletGeneric drugs (ANDA)May 16, 2025
Safeway1tabletGeneric drugs (ANDA)July 15, 2019
Sambrosa Care, Inc.1syrupOver the counter monograph drugsJanuary 10, 2020
Select Consumer Group1tabletGeneric drugs (ANDA)March 1, 2021
Strategic Sourcing Services LLC1tabletGeneric drugs (ANDA)May 3, 2023
Target Corporation1tabletGeneric drugs (ANDA)February 4, 2022
The Procter & Gamble Manufacturing Company1tabletGeneric drugs (ANDA)March 1, 2021
Topco Associates LLC1tabletGeneric drugs (ANDA)January 29, 1997
United Natural Foods, Inc. DBA Unfi1tabletGeneric drugs (ANDA)June 30, 2019
Wal-Mart Stores Inc1tabletGeneric drugs (ANDA)July 15, 2019
Yyba Corp1tabletGeneric drugs (ANDA)August 3, 2021

Dosage forms

Dosage formProductsShare
Tablet4686.8%
Liquid35.7%
Tablet, coated23.8%
Syrup11.9%
Capsule, liquid filled11.9%

Marketing categories

Marketing categoryProductsShare
Generic drugs (ANDA)4686.8%
Over the counter monograph drugs713.2%

Pharmacologic classes

ClassProducts
Antihistamine53

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.