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Data / Drug companies / Acetaminophen, doxylamine succinate, dextromethorphan hbr

Acetaminophen, doxylamine succinate, dextromethorphan hbr: 5 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, doxylamine succinate, dextromethorphan hbr is listed in the FDA National Drug Code Directory by 5 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 capsule, liquid filled; kit, and the newest product started marketing on August 17, 2026.

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Companies listing it
5
Products
6
Generic (ANDA) products
0 (0.0%)
Application numbers
1
Routes
Oral
Brand names
Vicks NyQuil Intense Flu Rapid Release LiquiCaps, Vicks DayQuil and Vicks NyQuil Intense Flu Rapid Release LiquiCaps, Multi-Symptom Nighttime Cold and Flu Relief, Night-Time Cold and Flu Relief, Nighttime Cold and Flu Relief, Nighttime Cold and Flu
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Companies that list acetaminophen, doxylamine succinate, dextromethorphan hbr

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

CompanyProductsMain dosage formsMain marketing categoryNewest product started
The Procter & Gamble Manufacturing Company2capsule, liquid filled; kitOver the counter monograph drugsAugust 17, 2026
Advanced Rx LLC1capsule, liquid filledOver the counter monograph drugsJanuary 1, 2025
Bi-Mart1capsule, liquid filledOver the counter monograph drugsMarch 1, 2025
Health Pharma USA LLC1capsule, liquid filledOver the counter monograph drugsDecember 20, 2024
HealthLife of USA LLC1capsule, liquid filledOver the counter monograph drugsApril 4, 2023

Dosage forms

Dosage formProductsShare
Capsule, liquid filled583.3%
Kit116.7%

Marketing categories

Marketing categoryProductsShare
Over the counter monograph drugs6100%

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.