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
- 0573-0165_4cd840a6-9554-de58-e063-6394a90ab543
- Product NDC
- 0573-0165
- Form
- TABLET, COATED
- Composition / generic term
- ibuprofen
- Labeler
- Haleon US Holdings LLC
- Marketing category
- NDA
- Marketing start / end (source format)
- 19840518
- Source listing expiry
- 20271231
Source-listed ingredients
- IBUPROFEN — 200 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE in 1 CARTON (0573-0165-20) / 24 TABLET, COATED in 1 BOTTLE · 0573-0165-20
- 1 BOTTLE in 1 CARTON (0573-0165-25) / 36 TABLET, COATED in 1 BOTTLE · 0573-0165-25
- 1 BOTTLE in 1 CARTON (0573-0165-30) / 50 TABLET, COATED in 1 BOTTLE · 0573-0165-30
- 1 BOTTLE in 1 CARTON (0573-0165-31) / 75 TABLET, COATED in 1 BOTTLE · 0573-0165-31
- 1 BOTTLE in 1 CARTON (0573-0165-40) / 100 TABLET, COATED in 1 BOTTLE · 0573-0165-40
- 1 BOTTLE in 1 CARTON (0573-0165-41) / 125 TABLET, COATED in 1 BOTTLE · 0573-0165-41
- 1 BOTTLE in 1 CARTON (0573-0165-42) / 150 TABLET, COATED in 1 BOTTLE · 0573-0165-42
Source and coverage
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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.
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