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
- 85237-1786_55bc239c-85cc-cd1c-e063-6394a90a8038
- Product NDC
- 85237-1786
- Form
- TABLET, COATED
- Composition / generic term
- ibuprofen
- Labeler
- Select Consumer Group
- 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 POUCH in 1 BLISTER PACK (85237-1786-1) / 1 TABLET, COATED in 1 POUCH · 85237-1786-1
- 2 POUCH in 1 BLISTER PACK (85237-1786-2) / 2 TABLET, COATED in 1 POUCH (85237-1786-0) · 85237-1786-2
- 25 POUCH in 1 BOX (85237-1786-4) / 2 TABLET, COATED in 1 POUCH (85237-1786-0) · 85237-1786-4
- 50 POUCH in 1 BOX (85237-1786-6) / 2 TABLET, COATED in 1 POUCH (85237-1786-0) · 85237-1786-6
- 3 POUCH in 1 BLISTER PACK (85237-1786-7) / 2 TABLET, COATED in 1 POUCH (85237-1786-0) · 85237-1786-7
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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