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
50844-292_310ac7c5-2530-4013-9f56-934a58054bd1
Product NDC
50844-292
Form
TABLET, FILM COATED
Composition / generic term
ibuprofen
Labeler
L.N.K. International, Inc.
Marketing category
ANDA
Marketing start / end (source format)
19880524
Source listing expiry
20271231

Source-listed ingredients

  • IBUPROFEN — 200 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 250 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-292-00) · 50844-292-00
  • 1 BOTTLE, PLASTIC in 1 CARTON (50844-292-01) / 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC · 50844-292-01
  • 1 BOTTLE, PLASTIC in 1 CARTON (50844-292-02) / 12 TABLET, FILM COATED in 1 BOTTLE, PLASTIC · 50844-292-02
  • 1 BOTTLE, PLASTIC in 1 CARTON (50844-292-08) / 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC · 50844-292-08
  • 1 BOTTLE, PLASTIC in 1 CARTON (50844-292-11) / 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC · 50844-292-11
  • 1 BOTTLE, PLASTIC in 1 CARTON (50844-292-12) / 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC · 50844-292-12
  • 1 BOTTLE, PLASTIC in 1 CARTON (50844-292-13) / 250 TABLET, FILM COATED in 1 BOTTLE, PLASTIC · 50844-292-13
  • 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-292-14) · 50844-292-14
  • 1 BOTTLE, PLASTIC in 1 CARTON (50844-292-15) / 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC · 50844-292-15
  • 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-292-16) · 50844-292-16

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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