United States· US:24208-377_4cb37a53-376f-ef57-e063-6294a90a5bf8

MIEBO

A medicinal product containing perfluorohexyloctane, registered in United States by Bausch & Lomb Incorporated.

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…normalisedMIEBOATC—REGISTER NO.US:24208-377_4cb37a53…PACKS LISTED6CHECKEDSeptember 27, 2026

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
PERFLUOROHEXYLOCTANE
Manufacturer
Bausch & Lomb Incorporated
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 · 6

  • ndc11
    2420837701
    1 BOTTLE in 1 CARTON (24208-377-01) / 3 mg in 1 BOTTLE
  • ndc11
    2420837705
    1 BOTTLE in 1 CARTON (24208-377-05) / 3 mg in 1 BOTTLE
  • ndc11
    2420837706
    1 BOTTLE in 1 CARTON (24208-377-06) / 1.6 mg in 1 BOTTLE
  • ndc11
    24208-377-01
  • ndc11
    24208-377-05
  • ndc11
    24208-377-06

Regulatory notes

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

Same medicine, other countries

Perfluorohexyloctane in 2 other countries

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

All perfluorohexyloctane 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/c0b0a7f4-d56b-4df6-bec5-15c0a0a171e8
GET /v1/drugs/c0b0a7f4-d56b-4df6-bec5-15c0a0a171e8?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": "OPHTHALMIC",
  "source": "ndc",
  "strength": "1",
  "substance": "PERFLUOROHEXYLOCTANE",
  "productndc": "24208-377",
  "dosage_form": "SOLUTION",
  "dea_schedule": null,
  "strength_unit": "mg/mg",
  "application_number": "NDA216675",
  "marketing_category": "NDA"
}

See everything about perfluorohexyloctane.

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.