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Acetaminophen 325 MG / dextromethorphan hydrobromide 10 MG Chewable Tablet — RxCUI 2685209

Name: Acetaminophen 325 MG / dextromethorphan hydrobromide 10 MG Chewable Tablet (RxCUI 2685209)
Creator: Brian Staiger, PharmD

RxNorm drug concept · Semantic clinical drug

RxCUI 2685209 Semantic clinical drug · SCD ● Current RxNorm concept 1 FDA product 2 package NDCs Snapshot Jul 14, 2026

This page is curated, coded, and maintained by Dr. Brian Staiger, PharmD

Compiled from public NLM RxNorm and FDA (openFDA NDC directory) data sources. Editorial policy

What you’re looking at: the standardized identity of one medicine, as the U.S. drug-data system sees it. Below — every FDA-listed product, package code, price benchmark, and billing code that maps to it.

🗂️ Key Facts

RxCUI2685209

Official nameAcetaminophen 325 MG / dextromethorphan hydrobromide 10 MG Chewable Tablet

Concept typeSemantic clinical drug (SCD)

RxNorm statusCurrent RxNorm concept

Also known asAPAP 325 MG / dextromethorphan hydrobromide 10 MG Chewable Tablet

FDA products mapped1

Package NDCs mapped2

RxNorm release07/06/2026

Snapshot dataJul 14, 2026

📖 Skip the Codes — Read It in Plain English.

Our pharmacist-built guide to Acetaminophen Injection: what it is, how it’s used, side effects, and interactions.

📗 Our plain-language guide HelloPharmacist

It treats mild to moderate pain, and moderate to severe pain when used with opioid medicines. It also lowers fever. It is given through a vein in a healthcare setting.
What is Acetaminophen Injection used for?
It is given as an IV infusion over 15 minutes by a healthcare professional. Your dose depends on your age and weight. Your care team follows the label and your prescriber's orders.
The most common are nausea and vomiting. Adults may also get headache or trouble sleeping. Children may have constipation or itching.

📖 Read our full Acetaminophen Injection guide →

🕸️ Concept Web — How Acetaminophen 325 MG / dextromethorphan hydrobro... Connects

One RxCUI never lives alone. Follow the path from the raw ingredient down to the exact strength-and-form concepts FDA products carry — every stop is a real RxNorm concept with its own identifier. Hover or focus any chip for what it means.

This page's concept Acetaminophen 325 MG / dextromethorphan hydrobromide 10 MG Chewable Tablet RxCUI 2685209 Semantic clinical drug · SCD

Every web starts here: one RxCUI, one fixed meaning in the RxNorm vocabulary.

Ingredients 4

The active substance itself — no strength, form, or brand attached yet.
- Acetaminophen 161 IN
- Dextromethorphan 3289 IN
- Acetaminophen / dextromethorphan 214180 MIN
- Dextromethorphan hydrobromide 102490 PIN
Dose forms 12

The ingredient poured into a form — tablet, solution, cream — still without one fixed strength.
- Acetaminophen / dextromethorphan Chewable Tablet 617729 SCDF
- Acetaminophen / dextromethorphan hydrobromide Chewable Tablet 2648893 SCDFP
- Acetaminophen / dextromethorphan Chewable Product 1295278 SCDG
- Acetaminophen / dextromethorphan Oral Product 1151184 SCDG
- Acetaminophen / dextromethorphan Pill 1151185 SCDG
- Acetaminophen / dextromethorphan hydrobromide Chewable Product 2660550 SCDGP
- Acetaminophen / dextromethorphan hydrobromide Oral Product 2662804 SCDGP
- Acetaminophen / dextromethorphan hydrobromide Pill 2662808 SCDGP
- +4 more in this family
Clinical & branded drugs 2

Ingredient + strength + dose form. These are the concepts real FDA products actually carry.
- Acetaminophen 325 MG 315263 SCDC
- Dextromethorphan hydrobromide 10 MG 1014455 SCDC

Showing up to 8 concepts per family — 14 of 18 stored related concepts drawn.

These are official RxNorm vocabulary relationships — how concepts name and organize the same medicine. They do not establish therapeutic equivalence or substitutability: two concepts appearing in one web is never a statement that products can be swapped.

🔀 Generic ⇄ Brand Crosswalk

The same medicine has an unbranded (generic) identity and one or more brand-name identities — each with its own RxCUI. This is a naming relationship in RxNorm, not a statement that any two products are substitutable.

Generic (Clinical) Concepts

Acetaminophen 325 MG SCDC · 315263
Dextromethorphan hydrobromide 10 MG SCDC · 1014455
Acetaminophen / dextromethorphan Chewable Tablet SCDF · 617729
Acetaminophen / dextromethorphan hydrobromide Chewable Tablet SCDFP · 2648893
Acetaminophen / dextromethorphan Chewable Product SCDG · 1295278
Acetaminophen / dextromethorphan Oral Product SCDG · 1151184
Acetaminophen / dextromethorphan Pill SCDG · 1151185
Acetaminophen / dextromethorphan hydrobromide Chewable Product SCDGP · 2660550
Acetaminophen / dextromethorphan hydrobromide Oral Product SCDGP · 2662804
Acetaminophen / dextromethorphan hydrobromide Pill SCDGP · 2662808

📦 FDA Products & Package NDCs

1 product · 2 package NDCs

2 package NDCs map to RxCUI 2685209 in the current snapshot — up to 50 per page. Each linked NDC opens its full package page.

Package NDC	Package	Brand / generic name	Labeler	Marketing start
00067-0111-01	20 TABLET, CHEWABLE in 1 BOTTLE (0067-0111-01)	Theraflu Severe Cold Relief Soft Chews	Haleon US Holdings LLC	2024-06-19
00067-0111-02	10 TABLET, CHEWABLE in 1 BOTTLE (0067-0111-02)	Theraflu Severe Cold Relief Soft Chews	Haleon US Holdings LLC	2024-06-19

Observed labelers: Haleon US Holdings LLC (2) — this is the FDA-listed mapping footprint, not sales, inventory, availability, or market share.

🗃️ Sources & Limits

Atlas generation902fddb9-e9c1-4004-bf4c-dba4d51037c7

openFDA export observedJul 14, 2026

RxNorm release07/06/2026

Methodology2026-07-full-catalog-v1

A shared RxCUI does not prove interchangeability. Products mapped to the same concept are not thereby equivalent or substitutable — equivalence is a separate, product-level determination.
Listing here does not establish approval or coverage. Appearing in this snapshot is a data observation, not an FDA approval status or a payer coverage decision.
Missing data never means zero. A silent dataset (no price, no billing code, no utilization) means no observation — not that the real-world value is zero.
Counts describe the mapping footprint. Product, package, and labeler counts are the FDA-listed mapping footprint in this snapshot — not sales, inventory, availability, or market share.

This product uses publicly available data from the U.S. National Library of Medicine (NLM), National Institutes of Health, Department of Health and Human Services; NLM is not responsible for the product and does not endorse or recommend this or any other product.

Machine-readable JSON

Reference information about drug-concept identifiers and public regulatory data — not medical advice. Talk to your pharmacist or prescriber about your own medication.