United States· US:0409-6695_3f83ed21-1b60-486c-8c70-1d5aa7553404
Amidate
A etomidate product containing etomidate, registered in United States by Hospira, Inc.. The same ATC class is registered in 12 of our 19 countries.
Checked against FDA National Drug Code directory (United States) on
Informational only — not a medical device.
Where it is registered
Etomidate is registered in 12 of 19 countries.
Countries holding a registration under ATC N01AX07 (etomidate), each read from that country’s own register.
- This record: United States, from FDA National Drug Code directory (United States)
- 8 of them publish a price we can compare per daily dose
Etomidate · ATC N01AX07
12 / 19 countries
- Belgiumprice
- Canada
- Czechiaprice
- Franceprice
- Germany
- Netherlands
- Norwayprice
- Polandprice
- Spainprice
- Switzerlandprice
- United Kingdom
- United Statesprice
The record
At a glance
FDA National Drug Code directory (United States)- Active substance
- ETOMIDATE
- Manufacturer
- Hospira, Inc.
- Country
- United States (US)
- ATC code
- N01AX07
- ATC class
- Etomidate
- Reimbursed
- Not published by this register
- Source register
- FDA National Drug Code directory (United States)
- Last checked
- September 27, 2026
Packs & prices · 4
- ndc11040966950110 VIAL, SINGLE-DOSE in 1 TRAY (0409-6695-01) / 10 mL in 1 VIAL, SINGLE-DOSE (0409-6695-11)
- ndc11040966950210 VIAL, SINGLE-DOSE in 1 TRAY (0409-6695-02) / 20 mL in 1 VIAL, SINGLE-DOSE (0409-6695-12)
- ndc110409-6695-01
- ndc110409-6695-02
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Interactions
59 interactions on record for etomidate.
Graded by severity as the source publishes them — 4 moderate. Severity grades are free for everyone; mechanism and management come with Growth.
- Severity for every pair — free, no plan needed
- The source, licence and sync date on every record
- Mechanism and what to do for each pair — Growth plan
Etomidate · interactions on record
59 records
- 4 moderate
- 55 info
Most severe, free to view
- EthanolB05XX04moderate
- EthanolV03AB16moderate
- EthanolV03AZ01moderate
- EthanolV07AB03moderate
- Interaction severity from DDInter 2.0 (Xiong G. et al., Nucleic Acids Res.), licensed CC BY-NC 4.0 — free for non-commercial use only; not covered by the Drug Database commercial licence.
Same medicine, other countries
Etomidate in 11 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- PolandEtomidate-LipuroB. Braun Melsungen AG
- United KingdomEtomidate 20mg/10ml emulsion for injection ampoulesB.Braun Medical Ltd
- CanadaETOMIDATE INJECTION USPMARCAN PHARMACEUTICALS INC
- BelgiumEtomidate - Lipuro 20 mg/10 mlB. Braun Melsungen
- NetherlandsEtomidaat-Lipuro 2 mg/ml, emulsie voor injectieB. Braun Melsungen AG (Melsungen)
- NorwayEtomidat-LipuroB. Braun
- FranceETOMIDATE LIPURO 20 mg/10 ml, émulsion injectableB BRAUN MELSUNGEN
- CzechiaHYPNOMIDATEPiramal Critical Care B.V., Voorschoten
Authorised across Europe · EMA
The same active substance is authorised in 15 EEA countries. Names it is sold under:
- Austria · Etomidat-Lipuro B. Braun Melsungen, Hypnomidate
- Belgium · Etomidate-Lipuro B. Braun Melsungen, Hypnomidate
- Czechia · Hypnomidate
- Germany · Etomidat-Lipuro B. Braun Melsungen, Hypnomidate
- Spain · Etomidato-Lipuro B.Braun Melsungen, Hypnomidate
- France · Etomidate Lipuro B. Braun Melsungen, Hypnomidate
- United Kingdom (Northern Ireland) · Etomidate-Lipuro B. Braun Melsungen, Hypnomidate
- Croatia · Hypnomidate
- Hungary · Etomidat-Lipuro B. Braun Melsungen
- Lithuania · Etomidate Braun
- Luxembourg · Etomidat-Lipuro B. Braun Melsungen, Hypnomidate
- Netherlands · Etomidaat Lipuro B.Braun Melsungen, Hypnomidate
- Poland · Etomidate-Lipuro B. Braun Melsungen, Hypnomidate
- Portugal · Etomidato-Lipuro B. Braun Medical
- Romania · Etomidat - Lipuro B. Braun Melsungen
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/cf81b5ce-f2d7-43b3-a3db-765c2848b097 GET /v1/drugs/cf81b5ce-f2d7-43b3-a3db-765c2848b097?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": "INTRAVENOUS",
"source": "ndc",
"strength": "2",
"substance": "ETOMIDATE",
"productndc": "0409-6695",
"dosage_form": "INJECTION, SOLUTION",
"dea_schedule": null,
"strength_unit": "mg/mL",
"application_number": "NDA018227",
"marketing_category": "NDA"
}See everything about etomidate.
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.