United States · FDA National Drug Code directory

Rufinamide

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
60687-824_5aa99d72-bc7f-1ea4-e063-6294a90a119e
Product NDC
60687-824
Form
SUSPENSION
Composition / generic term
Rufinamide
Labeler
American Health Packaging
Marketing category
ANDA
Marketing start / end (source format)
20260106 / 20270531

Source-listed ingredients

  • RUFINAMIDE — 40 mg/mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 3 TRAY in 1 CASE (60687-824-08) / 10 CUP, UNIT-DOSE in 1 TRAY (60687-824-48) / 10 mL in 1 CUP, UNIT-DOSE (60687-824-42) · 60687-824-08

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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