United States· US:80425-0517_346855a0-df4e-6369-e063-6394a90a0737

Diclona

A medicinal product containing diclofenac sodium; lidocaine, registered in United States by Advanced Rx of Tennessee, LLC.

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…normalisedDiclonaATC—REGISTER NO.US:80425-0517_346855a…PACKS LISTED2CHECKEDSeptember 27, 2026

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
DICLOFENAC SODIUM; LIDOCAINE
Manufacturer
Advanced Rx of Tennessee, LLC
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
    8042505171
    99 g in 1 TUBE (80425-0517-1)
  • ndc11
    80425-0517-1

Regulatory notes

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

Same medicine, other countries

Diclofenac sodium; lidocaine in 3 other countries

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

All diclofenac sodium; lidocaine products

Authorised across Europe · EMA

The same active substance is authorised in 5 EEA countries. Names it is sold under:

  • Germany · Diclofenac Ratiopharm
  • Lithuania · Olfen
  • Luxembourg · Diclofenac Ratiopharm®
  • Latvia · Olfen
  • Poland · Olfen 75

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/4771f6de-d536-457e-8869-6752071ff5ee
GET /v1/drugs/4771f6de-d536-457e-8869-6752071ff5ee?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": "CUTANEOUS",
  "source": "ndc",
  "strength": ".01; .045",
  "substance": "DICLOFENAC SODIUM; LIDOCAINE",
  "productndc": "80425-0517",
  "dosage_form": "GEL",
  "dea_schedule": null,
  "strength_unit": "g/g; g/g",
  "application_number": null,
  "marketing_category": "UNAPPROVED DRUG OTHER"
}

See everything about diclofenac sodium; lidocaine.

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.