United States· US:0071-0525_5d3eee75-8d10-4969-b883-81b1d5d3ae97

Celontin

A medicinal product containing methsuximide, registered in United States by Parke-Davis Div of Pfizer Inc.

US label

Checked against FDA National Drug Code directory (United States) on

Informational only — not a medical device.

SOURCE REGISTER · USFDA National Drug Code directory (Unite…normalisedCelontinATC—REGISTER NO.US:0071-0525_5d3eee75…PACKS LISTED2CHECKEDSeptember 27, 2026

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
METHSUXIMIDE
Manufacturer
Parke-Davis Div of Pfizer Inc
Country
United States (US)
ATC code
—
Reimbursed
Not published by this register
Source register
FDA National Drug Code directory (United States)
Last checked
September 27, 2026

Packs & prices · 2

  • ndc11
    0071052524
    100 CAPSULE in 1 BOTTLE (0071-0525-24)
  • ndc11
    0071-0525-24

Regulatory notes

No shortage, Orange Book or US label notes for this record.

Same medicine, other countries

Methsuximide in 3 other countries

What each register calls a product with the same active substance — salts and hydrates count as the same.

All methsuximide products

Authorised across Europe · EMA

The same active substance is authorised in 1 EEA country. Names it is sold under:

  • Germany · Petinutin

Source: European Medicines Agency, Article 57 product data.

Sourced from a public register and reproduced with attribution. Drug Database is not affiliated with, endorsed by, or a partner of FDA National Drug Code directory (United States). This is an informational data service and not a medical device — verify against the official source of record before any clinical decision.

For developers

The same record over the API, and the raw payload
GET /v1/drugs/52bf06a4-bb35-40b7-9154-c84ee13f2581
GET /v1/drugs/52bf06a4-bb35-40b7-9154-c84ee13f2581?format=fhir

Every response carries last_synced_at, so freshness is a field rather than a promise. Below is exactly what the ingestion wrote, before any presentation — the same JSON the API returns under payload.

{
  "route": "ORAL",
  "source": "ndc",
  "strength": "300",
  "substance": "METHSUXIMIDE",
  "productndc": "0071-0525",
  "dosage_form": "CAPSULE",
  "dea_schedule": null,
  "strength_unit": "mg/1",
  "application_number": "NDA010596",
  "marketing_category": "NDA"
}

See everything about methsuximide.

This page is the registration. A free account adds the label text as the regulator wrote it, what it costs per daily dose across the markets that publish a price, a feed of what changes in the registers, and an assistant that answers with its sources. Interaction severity is free; mechanism and management are on the Growth plan. No card, nothing to install.