United States · FDA National Drug Code directory
Ibuprofen
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
- 82804-227_67101108-a41f-4be1-8160-6a817c4c301e
- Product NDC
- 82804-227
- Form
- TABLET, FILM COATED
- Composition / generic term
- Ibuprofen
- Labeler
- Proficient Rx LP
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20240523
- Source listing expiry
- 20271231
Source-listed ingredients
- IBUPROFEN — 800 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 15 TABLET, FILM COATED in 1 BOTTLE (82804-227-15) · 82804-227-15
- 20 TABLET, FILM COATED in 1 BOTTLE (82804-227-20) · 82804-227-20
- 21 TABLET, FILM COATED in 1 BOTTLE (82804-227-21) · 82804-227-21
- 30 TABLET, FILM COATED in 1 BOTTLE (82804-227-30) · 82804-227-30
- 60 TABLET, FILM COATED in 1 BOTTLE (82804-227-60) · 82804-227-60
- 90 TABLET, FILM COATED in 1 BOTTLE (82804-227-90) · 82804-227-90
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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