United States· US:68462-659_ecbea621-93b0-40ce-adce-1d304c4fdb15

Ryaltris

A medicinal product containing olopatadine hydrochloride; mometasone furoate monohydrate, registered in United States by Glenmark Pharmaceuticals Inc., USA.

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

Informational only — not a medical device.

SOURCE REGISTER · USFDA National Drug Code directory (Unite…normalisedRyaltrisATC—REGISTER NO.US:68462-659_ecbea621…PACKS LISTED2CHECKEDSeptember 27, 2026

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
OLOPATADINE HYDROCHLORIDE; MOMETASONE FUROATE MONOHYDRATE
Manufacturer
Glenmark Pharmaceuticals Inc., USA
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
    68462-659-27
  • ndc11
    68462-659-84

Regulatory notes

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

Same medicine, other countries

Olopatadine hydrochloride; mometasone furoate monohydrate in 13 other countries

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

All olopatadine hydrochloride; mometasone furoate monohydrate products

Authorised across Europe · EMA

The same active substance is authorised in 21 EEA countries. Names it is sold under:

  • Austria · Ryaltris
  • Belgium · Ryaltris
  • Czechia · Ryaltris
  • Germany · Ryaltris
  • Denmark · Ryaltris
  • Spain · Ryaltris
  • Finland · Ryaltris
  • France · Ryaltris
  • United Kingdom (Northern Ireland) · Ryaltris
  • Ireland · Ryaltris
  • Italy · Rineffix, Ryaltris
  • Lithuania · Ryaltris
  • Luxembourg · Ryaltris
  • Latvia · Ryaltris
  • Malta · Ryaltris
  • Netherlands · Ryaltris
  • Norway · Ryaltris
  • Poland · Ryaltris
  • Romania · Ryaltris
  • Sweden · Mometasone Furoate/Olopatadine Glenmark, Ryaltris
  • Slovakia · Ryaltris

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/22d72bbf-c9d4-4b01-bacc-80d25cfe51a8
GET /v1/drugs/22d72bbf-c9d4-4b01-bacc-80d25cfe51a8?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": "NASAL",
  "source": "ndc",
  "strength": "665; 25",
  "substance": "OLOPATADINE HYDROCHLORIDE; MOMETASONE FUROATE MONOHYDRATE",
  "productndc": "68462-659",
  "dosage_form": "SPRAY, METERED",
  "dea_schedule": null,
  "strength_unit": "ug/1; ug/1",
  "application_number": "NDA211746",
  "marketing_category": "NDA"
}

See everything about olopatadine hydrochloride; mometasone furoate monohydrate.

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.