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United States· US:72189-320_32d607f3-fd60-9098-e063-6294a90a57af

NEOMYCIN POLYMYXIN B SULFATES AND DEXAMETHASONE

A medicinal product containing neomycin sulfate; polymyxin b sulfate; dexamethasone, registered in United States by DirectRx.

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…normalisedNEOMYCIN POLYMYXIN B SULFATES AND DEX…ATC—REGISTER NO.US:72189-320_32d607f3…PACKS LISTED2CHECKEDSeptember 27, 2026

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
NEOMYCIN SULFATE; POLYMYXIN B SULFATE; DEXAMETHASONE
Manufacturer
DirectRx
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
    72189-320-05
  • ndc11
    7218932005
    5 mL in 1 BOTTLE (72189-320-05)

Regulatory notes

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

Same medicine, other countries

Neomycin sulfate; polymyxin b sulfate; dexamethasone in 5 other countries

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

All neomycin sulfate; polymyxin b sulfate; dexamethasone products

Authorised across Europe · EMA

The same active substance is authorised in 19 EEA countries. Names it is sold under:

  • Belgium · Maxitrol
  • Bulgaria · Макситрол, Неладекс
  • Cyprus · Isopto Maxitrol
  • Czechia · Maxitrol
  • Germany · Isopto-Max
  • Estonia · Maxitrol
  • Spain · Maxitrol
  • France · Maxidrol
  • United Kingdom (Northern Ireland) · Maxitrol
  • Croatia · Maxitrol
  • Ireland · Maxitrol
  • Iceland · Maxitrol
  • Lithuania · Maxitrol
  • Luxembourg · Maxitrol
  • Latvia · Maxitrol
  • Norway · Maxitrol
  • Poland · Maxitrol
  • Romania · Maxitrol
  • Slovenia · Maxitrol

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/f05e99ed-81b1-4605-bbdf-e8c20db3e6fe
GET /v1/drugs/f05e99ed-81b1-4605-bbdf-e8c20db3e6fe?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": "TOPICAL",
  "source": "ndc",
  "strength": "3.5; 10000; 1",
  "substance": "NEOMYCIN SULFATE; POLYMYXIN B SULFATE; DEXAMETHASONE",
  "productndc": "72189-320",
  "dosage_form": "SUSPENSION/ DROPS",
  "dea_schedule": null,
  "strength_unit": "mg/mL; [USP'U]/mL; mg/mL",
  "application_number": "ANDA064135",
  "marketing_category": "ANDA"
}

See everything about neomycin sulfate; polymyxin b sulfate; dexamethasone.

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.