Orange Book drug · Brand (NDA)

Advil Dual Action With Acetaminophen

Acetaminophen; Ibuprofen

RLDNDA 211733 Haleon US Holdings

Approved

Feb 28, 2020

Strengths

Listed patents

What does the FDA Orange Book show for Advil Dual Action With Acetaminophen?

Advil Dual Action With Acetaminophen contains Acetaminophen; Ibuprofen and is the new drug FDA Orange Book record for NDA 211733. The application has 1 presentation with strength, dosage-form, route, status, RLD/RS, TE, patent, and exclusivity context. Current inventory and clinical labeling are not established without an application-matched source.

FDA application: NDA 211733
Application holder: Haleon US Holdings LLC
Product presentations: 1
Marketing categories: Over-the-counter
Reference roles: RLD / RS
TE codes: None posted
Listed patents: 1
Exclusivity records: 0

Sourced from the official FDA Orange Book data file · snapshot refreshed Jul 02, 2026, 06:34 PM

FDA product-presentation matrix

Every product number in this exact application

Every FDA product presentation under this application, with strength, dosage form and route, marketing status, therapeutic-equivalence code, and reference role.
Product	Strength	Dosage form / route	Marketing status	TE code	Reference role
001	250MG;125MG	TABLETORAL	Over-the-counter	None posted	RLDRS

Marketing status, TE code, RLD, and RS are presentation-level fields. Never transfer one product number's designation to another presentation.

Who is responsible for this application?

Application holder is not the same as manufacturer

FDA application holder

Haleon US Holdings LLC

The Orange Book identifies this organization as the applicant responsible for NDA 211733.

Manufacturer status

Not established by the Orange Book

A product-specific FDA label or NDC source must independently identify a manufacturer, labeler, distributor, packager, repackager, or relabeler. The applicant name is not used as a substitute for that evidence.

Regulatory interpretation

What the record means, and what it does not

FDA marketing status

1 presentation listed as over-the-counter

RX and OTC are Orange Book marketing categories, not real-time inventory signals. Confirm current commercial availability with labeling, the application holder, or an authoritative drug listing.

Therapeutic equivalence

No TE code is posted for this application

No TE code does not mean FDA found the product ineffective or non-equivalent. FDA generally publishes TE evaluations for multisource prescription products; single-source and some other products may have no code.

Patent & exclusivity record

1 listed patent expiration and 0 exclusivity dates remain on or after Jul 26, 2026

The latest future date recorded across those files is Jul 09, 2041. Patent and FDA exclusivity operate independently, can overlap, and do not by themselves predict a generic launch date.

Same-ingredient landscape

10 other ANDAs and 1 other NDA found

9 of the related ANDA applications are not marked discontinued. Sharing an ingredient does not establish pharmaceutical or therapeutic equivalence; strength, dosage form, route, and TE group still matter.

Which products are meaningfully comparable?

Exact ingredient + dosage form + route cohorts

NDA 211733 appears in 1 comparison cohort. These groups narrow the same-ingredient landscape, but strength and TE code must still match before interpreting therapeutic equivalence.

Tablet · Oral

Acetaminophen; Ibuprofen

12 applications

Product rows: 12
Active applications: 11
Active with AB row: 0

Combogesic · NDA 209471 Acetaminophen And Ibuprofen · ANDA 219053 Acetaminophen And Ibuprofen · ANDA 220126 Acetaminophen And Ibuprofen · ANDA 217241 Acetaminophen And Ibuprofen · ANDA 218247 Acetaminophen And Ibuprofen · ANDA 218311

Why are clinical sections unavailable?

Exact application-label matching status

Exact source match queuedQueue NDA-211733

No exact application-level FDA or DailyMed label match has been reviewed for this application. Approved uses, dosing, warnings, adverse reactions, and clinical evidence remain unavailable rather than being inherited from a related brand, generic, or ingredient record.

Until an exact application match passes human review, this page intentionally omits approved uses, dosing, warnings, adverse reactions, mechanism, and clinical-study summaries. It never inherits those claims from an RLD, brand, generic, or same-ingredient product.

Product detail

NDA 211733

RLDRS

Strength: 250MG;125MG
Dosage form: TABLET
Route: ORAL
Marketing status: Over-the-counter

Key dates

Approval, patents, exclusivity

Approval
FDA approval date of this drug product.
Feb 28, 2020
6 yr 6 mo ago
Today
Patent 11918693 expires
Listed drug product patent expiration.
Jul 09, 2041
in 15 yr 2 mo

Patent & exclusivity timeline

Protection horizon

Patent expiryExclusivity endToday

Pharmaceutical detail

FDA product record

Active ingredient

ACETAMINOPHEN; IBUPROFEN

Strength

250MG;125MG

Dosage form

TABLET

Route

ORAL

TE code

Not listed

Application

NDA 211733

Product number

001

Marketing status

Over-the-counter

Reference listed drug (RLD)

Yes

Reference standard (RS)

Yes

Listed patents

Orange Book patent file

Patents listed in the FDA Orange Book for this product, with expiration date and patent type.
Patent	Expires	In	Type
11918693	Jul 09, 2041	in 15 yr 2 mo	Product

Active-ingredient family

Brand + generics

This is a reference-listed drug (RLD), the basis for generic (ANDA) applications. Other products sharing this ingredient are listed below.

View full Acetaminophen; Ibuprofen family

How to use this record responsibly

Scope, limitations, and primary sources

What to verify before making a decision

The applicant is the holder of legal responsibility for the application; the Orange Book does not establish that the applicant manufactured or currently markets every listed product.
RX, OTC, and discontinued are FDA listing categories, not real-time pharmacy inventory or commercial-availability data.
Therapeutic equivalence applies only within the matching ingredient, dosage form, route, strength, and TE-code group; same ingredient alone is insufficient.
Listed patent and exclusivity dates are regulatory intelligence, not legal advice, a freedom-to-operate analysis, or a reliable generic-launch forecast.
The Orange Book is not prescribing information and does not provide indications, dosing, contraindications, adverse reactions, recalls, or current safety communications.

Official FDA references

Data shown here is normalized for search and comparison. When a regulatory, substitution, launch, or legal decision turns on a field, verify it against the current FDA record and the relevant source document.