Acetaminophen 32.5 MG/ML / dextromethorphan hydrobromide 1 MG/ML / guaifenesin 20 MG/ML Or... — RxCUI 2680300
RxNorm drug concept · Semantic clinical drug
RxCUI 2680300
Semantic clinical drug · SCD
● Current RxNorm concept 10 FDA products
12 package NDCs
Snapshot Jul 14, 2026
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
RxCUI2680300
Official nameAcetaminophen 32.5 MG/ML / dextromethorphan hydrobromide 1 MG/ML / guaifenesin 20 MG/ML Oral Solution
Concept typeSemantic clinical drug (SCD)
RxNorm statusCurrent RxNorm concept
Also known asAPAP 32.5 MG/ML / dextromethorphan hydrobromide 1 MG/ML / guaifenesin 20 MG/ML Oral Solution; acetaminophen 650 MG / dextromethorphan HBr 20 MG / guaiFENesin 400 MG in 20 mL Oral Solution; acetaminophen 650 MG / dextromethorphan HBr 20 MG / guaifenesin 400 MG per 20 ML Oral Solution
FDA products mapped10
Package NDCs mapped12
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
- Great question. The IV form is used when you can't take medication by mouth — for example, after surgery, if you're nauseated, or if you need faster, more reliable absorption. It d...
- Why am I getting acetaminophen through an IV instead of just taking a pill?
- Yes, Acetaminophen Injection is approved for children — for pain relief in kids 2 years and older, and for fever reduction in patients of all ages, including premature newborns bor...
- The most important things to watch for are signs of a serious allergic reaction — swelling of your face, mouth, or throat, trouble breathing, or hives — and any new skin rash. Eith...
🕸️ Concept Web — How Acetaminophen 32.5 MG/ML / dextromethorphan hydr... 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 32.5 MG/ML / dextromethorphan hydrobromide 1 MG/ML / guaifenesin 20 MG/ML Oral Solution
RxCUI 2680300 Semantic clinical drug · SCD
Every web starts here: one RxCUI, one fixed meaning in the RxNorm vocabulary.
-
Ingredients 5
The active substance itself — no strength, form, or brand attached yet.
-
Acetaminophen
161IN -
Dextromethorphan
3289IN -
Guaifenesin
5032IN -
Acetaminophen / dextromethorphan / guaifenesin
689775MIN -
Dextromethorphan hydrobromide
102490PIN
-
Acetaminophen
-
Dose forms 9
The ingredient poured into a form — tablet, solution, cream — still without one fixed strength.
-
Acetaminophen / dextromethorphan / guaifenesin Oral Solution
375971SCDF -
Acetaminophen / dextromethorphan hydrobromide / guaifenesin Oral Solution
2646565SCDFP -
Acetaminophen / dextromethorphan / guaifenesin Oral Liquid Product
1155912SCDG -
Acetaminophen / dextromethorphan / guaifenesin Oral Product
1155913SCDG -
Acetaminophen / dextromethorphan hydrobromide / guaifenesin Oral Liquid Product
2659921SCDGP -
Acetaminophen / dextromethorphan hydrobromide / guaifenesin Oral Product
2662330SCDGP -
Oral Solution
316968DF -
Oral Liquid Product
1151137DFG - +1 more in this family
-
Acetaminophen / dextromethorphan / guaifenesin Oral Solution
-
Clinical & branded drugs 3
Ingredient + strength + dose form. These are the concepts real FDA products actually carry.
-
Acetaminophen 32.5 MG/ML
336021SCDC -
Dextromethorphan hydrobromide 1 MG/ML
1020137SCDC -
Guaifenesin 20 MG/ML
316011SCDC
-
Acetaminophen 32.5 MG/ML
Showing up to 8 concepts per family — 16 of 17 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 32.5 MG/ML
SCDC · 336021 -
Dextromethorphan hydrobromide 1 MG/ML
SCDC · 1020137 -
Guaifenesin 20 MG/ML
SCDC · 316011 -
Acetaminophen / dextromethorphan / guaifenesin Oral Solution
SCDF · 375971 -
Acetaminophen / dextromethorphan hydrobromide / guaifenesin Oral Solution
SCDFP · 2646565 -
Acetaminophen / dextromethorphan / guaifenesin Oral Liquid Product
SCDG · 1155912 -
Acetaminophen / dextromethorphan / guaifenesin Oral Product
SCDG · 1155913 -
Acetaminophen / dextromethorphan hydrobromide / guaifenesin Oral Liquid Product
SCDGP · 2659921 -
Acetaminophen / dextromethorphan hydrobromide / guaifenesin Oral Product
SCDGP · 2662330
📦 FDA Products & Package NDCs
10 products · 12 package NDCs
12 package NDCs map to RxCUI 2680300 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 |
|---|---|---|---|---|
| 00031-0100-04 | 1 BOTTLE in 1 CARTON (0031-0100-04) / 118 mL in 1 BOTTLE | Robitussin Maximum Strength Severe Multi-Symptom Cough Cold Flu | Haleon US Holdings LLC | 2024-02-15 |
| 00031-0100-08 | 1 BOTTLE in 1 CARTON (0031-0100-08) / 237 mL in 1 BOTTLE | Robitussin Maximum Strength Severe Multi-Symptom Cough Cold Flu | Haleon US Holdings LLC | 2024-02-15 |
| 00113-2009-34 | 1 BOTTLE in 1 CARTON (0113-2009-34) / 237 mL in 1 BOTTLE (0... | GOOD SENSE TUSSIN | L. Perrigo Company | 2026-01-08 |
| 11673-0794-01 | 1 KIT in 1 KIT (11673-794-01) * 177 mL in 1 BOTTLE, PLASTI... | Maximum Strength Daytime Severe and Nighttime Cold and Flu | TARGET Corporation | 2024-05-01 |
| 42507-0581-26 | 1 BOTTLE in 1 CARTON (42507-581-26) / 118 mL in 1 BOTTLE (4... | Tussin Severe | HyVee Inc | 2026-01-28 |
| 51316-0089-08 | 1 BOTTLE in 1 CARTON (51316-089-08) / 237 mL in 1 BOTTLE | CVS PHARMACY MS Adult Severe Multi Symptom Cough Cold Flu | CVS PHARMACY | 2025-06-23 |
| 51316-0189-26 | 1 BOTTLE in 1 CARTON (51316-189-26) / 118 mL in 1 BOTTLE | SEVERE COUGH COLD AND FLU | CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED | 2025-08-29 |
| 51316-0189-34 | 1 BOTTLE in 1 CARTON (51316-189-34) / 237 mL in 1 BOTTLE | SEVERE COUGH COLD AND FLU | CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED | 2025-08-29 |
| 57896-0596-08 | 237 mL in 1 BOTTLE (57896-596-08) | Geri Care Tussin CF Max | GERI-CARE PHARMACEUTICAL CORP | 2025-12-01 |
| 58593-0005-08 | 237 mL in 1 BOTTLE (58593-005-08) | Rompe Pecho Max | Efficient Laboratories Inc | 2026-06-01 |
| 70000-0739-01 | 1 BOTTLE in 1 CARTON (70000-0739-1) / 118 mL in 1 BOTTLE | LEADER TUSSIN CF | Cardinal Health 110, LLC. dba Leader | 2025-09-30 |
| 76162-0198-26 | 1 BOTTLE in 1 CARTON (76162-198-26) / 118 mL in 1 BOTTLE | TOPCARE TUSSIN CF MAX | Topco Associates LLC | 2026-02-11 |
Observed labelers:
CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED (2) ·
Haleon US Holdings LLC (2) ·
Cardinal Health 110, LLC. dba Leader (1) ·
CVS PHARMACY (1) ·
Efficient Laboratories Inc (1) ·
GERI-CARE PHARMACEUTICAL CORP (1)
· +4 more — 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.
Reference information about drug-concept identifiers and public regulatory data — not medical advice. Talk to your pharmacist or prescriber about your own medication.