United States · FDA National Drug Code directory

Flurbiprofen

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
64950-218_d3fa269f-43c4-4862-b4d2-ec5b04d050c8
Product NDC
64950-218
Form
TABLET
Composition / generic term
Flurbiprofen
Labeler
Genus Lifesciences
Marketing category
ANDA
Marketing start / end (source format)
20241101
Source listing expiry
20271231

Source-listed ingredients

  • FLURBIPROFEN — 100 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 100 TABLET in 1 BOTTLE (64950-218-10) · 64950-218-10

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.

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