United States · FDA National Drug Code directory

Zarontin

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
0071-0237_b5966080-3265-4027-b1f6-67af24097f18
Product NDC
0071-0237
Form
CAPSULE
Composition / generic term
Ethosuximide
Labeler
Parke-Davis Div of Pfizer Inc
Marketing category
NDA
Marketing start / end (source format)
20000922
Source listing expiry
20271231

Source-listed ingredients

  • ETHOSUXIMIDE — 250 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 100 CAPSULE in 1 BOTTLE (0071-0237-24) · 0071-0237-24

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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Zarontin — United States | Molindra Medicines