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
- 83324-056_c10b9cb5-fa7d-4e1b-916c-3449ba8e9ccd
- Product NDC
- 83324-056
- Form
- TABLET, FILM COATED
- Composition / generic term
- Ibuprofen
- Labeler
- Chain Drug Marketing Association, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20240813
- Source listing expiry
- 20271231
Source-listed ingredients
- IBUPROFEN — 200 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE, PLASTIC in 1 CARTON (83324-056-01) / 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC · 83324-056-01
- 1 BOTTLE, PLASTIC in 1 CARTON (83324-056-24) / 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC · 83324-056-24
- 1 BOTTLE, PLASTIC in 1 CARTON (83324-056-50) / 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC · 83324-056-50
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 →