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United States· US:79903-424_c78d594a-96c7-40ab-bbbf-51a353df8da1

EQUATE ALLERGY RELIEF D

A medicinal product containing fexofenadine hydrochloride; pseudoephedrine hydrochloride, registered in United States by WALMART INC..

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

Informational only — not a medical device.

SOURCE REGISTER · USFDA National Drug Code directory (Unite…normalisedEQUATE ALLERGY RELIEF DATC—REGISTER NO.US:79903-424_c78d594a…PACKS LISTED1CHECKEDSeptember 27, 2026

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
FEXOFENADINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE
Manufacturer
WALMART 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 · 1

  • ndc11
    79903-424-20

Regulatory notes

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

Same medicine, other countries

Fexofenadine hydrochloride; pseudoephedrine hydrochloride in 1 other country

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

All fexofenadine hydrochloride; pseudoephedrine hydrochloride 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/bb6255a9-862c-43b0-941b-0df9533d0e90
GET /v1/drugs/bb6255a9-862c-43b0-941b-0df9533d0e90?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": "60; 120",
  "substance": "FEXOFENADINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE",
  "productndc": "79903-424",
  "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE",
  "dea_schedule": null,
  "strength_unit": "mg/1; mg/1",
  "application_number": "ANDA216792",
  "marketing_category": "ANDA"
}

See everything about fexofenadine hydrochloride; pseudoephedrine hydrochloride.

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.