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
- 50844-392_bdfc7556-6210-4b0a-9177-a6e42f258699
- Product NDC
- 50844-392
- 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 (50844-392-02) / 12 TABLET, FILM COATED in 1 BOTTLE, PLASTIC · 50844-392-02
- 1 BOTTLE, PLASTIC in 1 CARTON (50844-392-08) / 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC · 50844-392-08
- 1 BOTTLE, PLASTIC in 1 CARTON (50844-392-12) / 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC · 50844-392-12
- 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-392-14) · 50844-392-14
- 1 BOTTLE, PLASTIC in 1 CARTON (50844-392-15) / 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC · 50844-392-15
- 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-392-16) · 50844-392-16
- 50 POUCH in 1 CARTON (50844-392-50) / 2 TABLET, FILM COATED in 1 POUCH (50844-392-24) · 50844-392-50
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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