United States· US:70069-601_abb9ea27-1536-41b3-b84e-839796fdf710
Proparacaine Hydrochloride
A medicinal product containing proparacaine hydrochloride, registered in United States by Somerset Therapeutics, LLC.
Checked against FDA National Drug Code directory (United States) on
Informational only — not a medical device.
The record
At a glance
FDA National Drug Code directory (United States)- Active substance
- PROPARACAINE HYDROCHLORIDE
- Manufacturer
- Somerset Therapeutics, 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
- ndc1170069601011 BOTTLE in 1 CARTON (70069-601-01) / 15 mL in 1 BOTTLE
- ndc1170069-601-01
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Proparacaine hydrochloride in 9 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- PolandAlcaineInPharm Sp. z o.o.
- IcelandAlcaineAlcon Nordic A/S
- NorwayAlcaineAlcon Nordic A/S
- GermanyProparakain-PosUrsapharm Arzneimittel Gmbh
- United KingdomMinims proxymetacaine 0.5% eye drops 0.5ml unit doseBausch & Lomb UK Ltd
- BelgiumAlcaine 0.5 %Alcon
- IrelandMinims Proxymetacaine hydrochloride 0.5% w/v, Eye Drops, SolutionBausch + Lomb Ireland Limited
- CanadaALCAINEALCON CANADA INC
Authorised across Europe · EMA
The same active substance is authorised in 12 EEA countries. Names it is sold under:
- Belgium · Alcaine
- Bulgaria · Алкаин
- Cyprus · Alcaine
- Germany · Proparakain-Pos
- United Kingdom (Northern Ireland) · Proxymetacaine Hydrochloride Minims Bausch & Lomb Uk
- Greece · Alcaine
- Ireland · Minims
- Iceland · Alcaine
- Lithuania · Alcaine
- Norway · Alcaine
- Poland · Alcaine
- Slovenia · Alcaine
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/bce8574f-3e9a-4433-9628-6db1085ec372 GET /v1/drugs/bce8574f-3e9a-4433-9628-6db1085ec372?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": "5",
"substance": "PROPARACAINE HYDROCHLORIDE",
"productndc": "70069-601",
"dosage_form": "SOLUTION/ DROPS",
"dea_schedule": null,
"strength_unit": "mg/mL",
"application_number": "ANDA215816",
"marketing_category": "ANDA"
}See everything about proparacaine 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.