United States · FDA National Drug Code directory

Ethosuximide

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
68999-064_53fe494e-ed69-2aad-e063-6294a90a70e4
Product NDC
68999-064
Form
SOLUTION
Composition / generic term
Ethosuximide
Labeler
Chartwell Governmental & Specialty RX, LLC.
Marketing category
ANDA
Marketing start / end (source format)
20031222
Source listing expiry
20271231

Source-listed ingredients

  • ETHOSUXIMIDE — 250 mg/5mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 2 TRAY in 1 BOX (68999-064-24) / 10 CUP in 1 TRAY / 5 mL in 1 CUP (68999-064-05) · 68999-064-24

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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