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
- 50844-353_5f8c5841-a57f-4394-bbc2-93fc48474282
- Product NDC
- 50844-353
- Form
- TABLET, FILM COATED
- Composition / generic term
- ibuprofen
- Labeler
- L.N.K. International, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 19990301
- 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 (50844-353-02) / 12 TABLET, FILM COATED in 1 BOTTLE, PLASTIC · 50844-353-02
- 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-353-16) · 50844-353-16
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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