United States · FDA National Drug Code directory
Advil
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 0573-0134_40429ef4-846a-eb4c-e063-6394a90ab7a9
- Product NDC
- 0573-0134
- Form
- TABLET, COATED
- Composition / generic term
- ibuprofen sodium
- Labeler
- Haleon US Holdings LLC
- Marketing category
- NDA
- Marketing start / end (source format)
- 20130708
- Source listing expiry
- 20261231
Source-listed ingredients
- IBUPROFEN SODIUM — 256 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE in 1 CARTON (0573-0134-20) / 20 TABLET, COATED in 1 BOTTLE · 0573-0134-20
- 1 BOTTLE in 1 CARTON (0573-0134-80) / 80 TABLET, COATED in 1 BOTTLE · 0573-0134-80
Source and coverage
Open FDA National Drug Code directory →
Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
Browse United States records →