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
- 0904-6747_dddfc800-cfd3-42d4-82e1-04414822fbfc
- Product NDC
- 0904-6747
- Form
- TABLET, FILM COATED
- Composition / generic term
- Ibuprofen
- Labeler
- Major Pharmaceuticals
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20180920
- Source listing expiry
- 20261231
Source-listed ingredients
- IBUPROFEN — 200 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE in 1 CARTON (0904-6747-24) / 24 TABLET, FILM COATED in 1 BOTTLE · 0904-6747-24
- 500 TABLET, FILM COATED in 1 BOTTLE (0904-6747-40) · 0904-6747-40
- 1 BOTTLE in 1 CARTON (0904-6747-51) / 50 TABLET, FILM COATED in 1 BOTTLE · 0904-6747-51
- 1 BOTTLE in 1 CARTON (0904-6747-59) / 100 TABLET, FILM COATED in 1 BOTTLE · 0904-6747-59
- 1 BOTTLE in 1 CARTON (0904-6747-70) / 250 TABLET, FILM COATED in 1 BOTTLE · 0904-6747-70
- 1000 TABLET, FILM COATED in 1 BOTTLE (0904-6747-80) · 0904-6747-80
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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