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
- 68998-109_374dc1c0-4246-b272-e063-6394a90a5a6b
- Product NDC
- 68998-109
- Form
- TABLET, COATED
- Composition / generic term
- Ibuprofen
- Labeler
- Marc Glassman, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20090601
- Source listing expiry
- 20261231
Source-listed ingredients
- IBUPROFEN — 200 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE, PLASTIC in 1 CARTON (68998-109-03) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC · 68998-109-03
- 500 TABLET, COATED in 1 BOTTLE, PLASTIC (68998-109-05) · 68998-109-05
- 250 TABLET, COATED in 1 BOTTLE, PLASTIC (68998-109-08) · 68998-109-08
- 2 BOTTLE, PLASTIC in 1 CARTON (68998-109-10) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC · 68998-109-10
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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