United States· US:52389-249_3287c676-c9cc-273e-e063-6294a90a9c9b

Diurex

A medicinal product containing pamabrom, registered in United States by Kobayashi Healthcare International, 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…normalisedDiurexATC—REGISTER NO.US:52389-249_3287c676…PACKS LISTED12CHECKEDSeptember 27, 2026

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
PAMABROM
Manufacturer
Kobayashi Healthcare International, 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 · 12

  • ndc11
    52389-249-10
  • ndc11
    5238924910
    4 BLISTER PACK in 1 CARTON (52389-249-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK
  • ndc11
    5238924924
    1 BLISTER PACK in 1 CARTON (52389-249-24) / 24 TABLET, FILM COATED in 1 BLISTER PACK
  • ndc11
    5238924930
    3 BLISTER PACK in 1 CARTON (52389-249-30) / 10 TABLET, FILM COATED in 1 BLISTER PACK
  • ndc11
    5238924948
    2 BLISTER PACK in 1 CARTON (52389-249-48) / 24 TABLET, FILM COATED in 1 BLISTER PACK
  • ndc11
    5238924950
    5 BLISTER PACK in 1 CARTON (52389-249-50) / 10 TABLET, FILM COATED in 1 BLISTER PACK
  • ndc11
    5238924972
    3 BLISTER PACK in 1 CARTON (52389-249-72) / 24 TABLET, FILM COATED in 1 BLISTER PACK
  • ndc11
    52389-249-24
  • ndc11
    52389-249-30
  • ndc11
    52389-249-48
  • ndc11
    52389-249-50
  • ndc11
    52389-249-72

Regulatory notes

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

Same medicine, other countries

Pamabrom in 1 other country

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

All pamabrom products

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/e1f8b003-0ee9-403e-81b7-eec5775ddf3b
GET /v1/drugs/e1f8b003-0ee9-403e-81b7-eec5775ddf3b?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": "50",
  "substance": "PAMABROM",
  "productndc": "52389-249",
  "dosage_form": "TABLET, FILM COATED",
  "dea_schedule": null,
  "strength_unit": "mg/1",
  "application_number": "M027",
  "marketing_category": "OTC MONOGRAPH DRUG"
}

See everything about pamabrom.

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.