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
- 67877-320_88237aae-0838-49f5-8129-0fd07722a772
- Product NDC
- 67877-320
- Form
- TABLET, FILM COATED
- Composition / generic term
- Ibuprofen
- Labeler
- Ascend Laboratories, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20151221
- Source listing expiry
- 20271231
Source-listed ingredients
- IBUPROFEN — 600 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, FILM COATED in 1 BOTTLE (67877-320-01) · 67877-320-01
- 500 TABLET, FILM COATED in 1 BOTTLE (67877-320-05) · 67877-320-05
- 30 TABLET, FILM COATED in 1 BOTTLE (67877-320-30) · 67877-320-30
- 50 TABLET, FILM COATED in 1 BOTTLE (67877-320-50) · 67877-320-50
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 →