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Etomidate

Etomidate is an intravenous general anesthetic used to start (induce) anesthesia and, in short procedures, to supplement weaker anesthetic agents.

Brand name Amidate
Drug class General Anesthetic
Rx Form 1
Dr. Brian Staiger, PharmD, BCPS
Reviewed by Last reviewed Jul 15, 2026 Content updated Oct 2, 2026
🧬 Where this information comes from Click to expand

The clinical label records used on this page are FDA-filed Structured Product Labeling (SPL) retrieved through openFDA. We identified 14 clinical label sets within the page’s selected clinical scope after exact ingredient or ingredient-combination matching and applicable route/form matching. Forms, routes, brands, labelers, strengths, and NDC product-record counts are built separately from matching FDA National Drug Code Directory records. The linked DailyMed document is a representative official source for verification, not the page’s only clinical source. View the linked label on DailyMed →

Etomidate at a glance The quick version — the full detail is in the Patient Information Guide below.
Dr. Brian Staiger, PharmD, BCPS
The Pharmacist’s Take By · Clinical pharmacist · Written

Etomidate (Amidate) is an anesthetic given into a vein that puts you to sleep at the start of surgery or a short procedure, an older standby, available generically, often chosen for higher-risk patients because it barely affects heart function. Most people tolerate it well, though it can sting in the vein, brief muscle twitching (myoclonus) as you go under is common, and some feel queasy afterward. It also lowers cortisol and aldosterone, the body's stress hormones, for up to 6 to 8 hours, so it is used only to start anesthesia, never for prolonged sedation. If you feel unusually weak afterward, tell your care team.

Clinical pearls

  • Etomidate has no pain-relieving effect, so it is paired with other drugs such as fentanyl, which change the dose needed.
  • Mention any liver disease such as cirrhosis, since a slower-clearing liver keeps etomidate active longer than usual.
  • Older adults with high blood pressure are more prone to drops in heart rate and blood pressure, so expect closer monitoring.
  • It is not advised for starting anesthesia before age 10, and long elective surgery under age 3 deserves a timing discussion.
How you get itPrescription only
Comes asInjection
Earliest FDA record1982
Companies listing it with the FDA12
FDA label last updatedMay 20, 2026
FDA’s strongest warning (boxed)None on the label

Patient information guide A plain-language walkthrough of Etomidate, written from its FDA label.

What Etomidate is used for

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Etomidate is an intravenous general anesthetic. It is used in the following ways:

  • Amidate (intravenous injection) is indicated to induce general anesthesia in adults and in children older than 10 years
  • Etomidate injection (intravenous) is indicated to induce general anesthesia in adults and in children older than 10 years
  • Amidate (intravenous) is indicated to supplement weaker anesthetic agents — such as nitrous oxide in oxygen — during short procedures like dilation and curettage or cervical conization in adult patients
  • Etomidate injection (intravenous) is similarly indicated to supplement weaker anesthetic agents during short adult procedures
  • Use for induction in children under age 10 is not recommended due to insufficient data
  • Supplemental use during longer procedures or in pediatric patients is not recommended

How Etomidate works

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Etomidate is a general anesthetic — it puts you into a state of unconsciousness — but it does not relieve pain on its own. When injected into a vein, it acts on the brain to produce anesthesia almost immediately, usually within one minute. It causes a temporary, proportional reduction in cerebral (brain) blood flow and brain oxygen use, and it typically lowers intracranial pressure (pressure inside the skull) for several minutes. One of its notable properties is that, at standard doses, it has very little effect on the heart and circulation, which makes it useful for patients who need careful cardiovascular management.

Etomidate also temporarily suppresses the adrenal glands' production of cortisol and aldosterone — the body's key stress hormones — for roughly 6 to 8 hours after an induction dose. This effect does not respond to ACTH (the hormone that normally triggers cortisol release), which is why prolonged or repeated dosing carries significant risk.

Etomidate dosage

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Etomidate is given only as an intravenous (IV) injection by trained anesthesia professionals in a clinical setting — it is never taken by mouth or self-administered at home. The injection is given slowly, over about 30 to 60 seconds, and the dose is carefully individualized for each patient based on body weight and other factors.

  • Older adults may need a lower dose
  • It is not intended for prolonged continuous infusion
  • When used to supplement anesthesia during a short procedure, smaller follow-up doses may be given, but these are also individualized
  • Other medications given during anesthesia — including fentanyl — can affect how much etomidate is needed; the care team manages this

Dosing details from the FDA-approved label

From the Etomidate prescribing information (“Dosage and Administration”). Doses are set by your prescriber for your product, condition, kidney function and age — never change a dose on your own.

  • Induction of anesthesia in adult patients and pediatric patients above the age of ten (10) years
    • Varies between 0.2 mg/kg and 0.6 mg/kg of body weight, individualized in each case
    • Usual dose is 0.3 mg/kg, injected over a period of 30 to 60 seconds
    • Geriatric patients may require reduced doses of etomidate
  • Induction of anesthesia in patients below the age of ten (10) years
    • There are inadequate data to make dosage recommendations
    • Such use is not recommended
  • Supplementing subpotent anesthetic agents, such as nitrous oxide, during short operative procedures in adult patients
    • Smaller increments of intravenous etomidate may be administered
    • Dosage usually smaller than the original induction dose, must be individualized
    • Insufficient data to support use for longer adult procedures or any procedures in pediatric patients; such use is not recommended
Read the label’s full dosing text

DOSAGE AND ADMINISTRATION Do not administer unless solution is clear and container is undamaged. Discard unused portion (see DOSAGE AND ADMINISTRATION ). Etomidate Injection is intended for administration only by the intravenous route (see CLINICAL PHARMACOLOGY ). The dose for induction of anesthesia in adult patients and in pediatric patients above the age of ten (10) years will vary between 0.2 mg/kg and 0.6 mg/kg of body weight, and it must be individualized in each case. The usual dose for induction in these patients is 0.3 mg/kg, injected over a period of 30 to 60 seconds. There are inadequate data to make dosage recommendations for induction of anesthesia in patients below the age of ten (10) years; therefore, such use is not recommended. Geriatric patients may require reduced doses of etomidate. Smaller increments of intravenous etomidate may be administered to adult patients during short operative procedures to supplement subpotent anesthetic agents, such as nitrous oxide. The dosage employed under these circumstances, although usually smaller than the original induction dose, must be individualized. There are insufficient data to support this use of etomidate for longer adult procedures or for any procedures in pediatric patients; therefore, such use is not recommended. The use of intravenous fentanyl and other neuroactive drugs employed during the conduct of anesthesia may alter the etomidate dosage requirements. Consult the prescribing information for all other such drugs before using. Premedication: Etomidate Injection is compatible with commonly administered pre-anesthetic medications, which may be employed as indicated. See also CLINICAL PHARMACOLOGY , ADVERSE REACTIONS , and dosage recommendations for maintenance of anesthesia. Etomidate Injection anesthesia does not significantly alter the usual dosage requirements of neuromuscular blocking agents employed for endotracheal intubation or other purposes shortly after induction of anesthesia. Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration, whenever solution and container permit. To prevent needle-stick injuries, needles should not be recapped, purposely bent, or broken by hand.

Read the full Dosage and Administration section on DailyMed →

Etomidate side effects

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The most common side effects of etomidate happen during or immediately after the injection:

Common side effects

  • Pain or burning at the injection site in the vein
  • Involuntary muscle movements or twitching (myoclonus) during induction
  • Hiccups
  • Nausea and/or vomiting after the procedure
  • Brief periods of irregular or rapid breathing
  • Short-lived changes in blood pressure or heart rate
  • Hiccups or snoring during induction
  • Brief changes in breathing — too fast, too slow, or a very short pause in breathing
  • Short-term changes in blood pressure or heart rate

When to get medical help

  • Call for immediate medical help if you experience severe low blood pressure or racing heart rate, which could signal a serious allergic (anaphylactoid) reaction
  • Tell your care team right away if you have trouble breathing, throat tightness, or laryngospasm (airway spasm) after the injection
  • Etomidate temporarily lowers the body's production of cortisol and aldosterone (stress hormones) for up to 6–8 hours — alert your care team if you feel unusually weak or unwell after your procedure
  • Older adults with high blood pressure are at higher risk of cardiac depression (reduced heart function) and should be monitored closely

Serious reactions — including laryngospasm (airway spasm), severe low blood pressure, or signs of an allergic reaction — require immediate medical attention and are managed by the anesthesia team on site.

Etomidate warnings and precautions

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  • Trained personnel only: Etomidate must be administered solely by clinicians trained in general anesthesia, with equipment available to manage any complications immediately.
  • No prolonged infusion: Because etomidate suppresses the production of cortisol and aldosterone (vital stress hormones) for 6–8 hours after a single dose — an effect that does not respond to ACTH — it must never be given as a prolonged continuous drip. Extended hormonal suppression poses serious risks.
  • Developing brain risk in young children: Anesthetic drugs that act on certain brain receptors may cause nerve-cell loss and possible long-term cognitive or behavioral effects when used in the developing brain. The vulnerable window is thought to run from the third trimester of pregnancy through roughly the first 3 years of life. Families and providers should carefully weigh the necessity and timing of elective procedures in very young children.
  • Older adults with high blood pressure: Elderly patients — particularly those with hypertension — face a higher risk of drops in heart rate and blood pressure (cardiac depression) with etomidate.
  • Liver disease: In patients with cirrhosis, etomidate stays active in the body roughly twice as long as in healthy individuals.

Etomidate interactions

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Etomidate is given in a controlled medical setting, so your anesthesia team manages interactions directly. The key ones to know about include:

  • Fentanyl and other neuroactive drugs: These can reduce how much etomidate is needed and may shorten recovery time — your care team will adjust doses accordingly
  • Neuromuscular blocking agents (drugs that relax muscles for breathing tube placement): etomidate does not significantly change the dose needed for these, but they are always used together under close supervision
  • Pre-anesthetic (premedication) drugs: Common premedications are generally compatible with etomidate, but the full medication list must be reviewed before your procedure

Not a complete list. The label covers the interactions the manufacturer studied or reported, and our own interaction database does not cover every medicine either. Bring your full medication list, including vitamins and herbal products, to your pharmacist.

Before taking Etomidate

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  • Allergy to etomidate: Etomidate is contraindicated (must not be used) in anyone with a known hypersensitivity (allergic reaction) to it — tell your team about any prior reactions
  • Children under 10: Etomidate is not recommended for induction of anesthesia in this age group due to insufficient safety data
  • Young children and pregnancy: Because of the potential for anesthetic drugs to affect the developing brain, parents and pregnant women should discuss the timing of any elective procedures with their doctor
  • Older adults, especially with high blood pressure: Greater risk of drops in blood pressure, heart rate, and cardiac output — dose adjustments and close monitoring are needed
  • Liver disease (cirrhosis): The drug is cleared more slowly, meaning effects may last longer
  • Severe trauma or very low blood volume: The cardiovascular response to etomidate in these situations is not well established — full disclosure of your condition to the care team is essential

Etomidate overdose

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An overdose of etomidate can occur if it is injected too rapidly or in repeated doses. Too fast an injection can cause a drop in blood pressure. If an overdose is suspected, the drug is stopped immediately, the airway is secured (with a breathing tube if necessary), and oxygen with assisted breathing is provided as needed.

What Etomidate does in the body

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Etomidate produces unconsciousness rapidly — usually within one minute — but provides no pain relief on its own. It causes a temporary 20–30% reduction in cerebral (brain) blood flow and a proportional reduction in brain oxygen use, and it typically lowers intracranial pressure (pressure inside the skull) for several minutes. At standard doses, it has little to no effect on the heart, cardiac output, or circulation, making it particularly useful in patients with cardiovascular disease. It also temporarily suppresses cortisol and aldosterone production by the adrenal glands for roughly 6 to 8 hours, an effect that does not respond to the body's normal hormonal signals.

How your body processes Etomidate

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After a single intravenous dose, etomidate takes effect within about one minute, and unconsciousness typically lasts only 3 to 5 minutes at a standard dose — making recovery relatively quick. The drug is rapidly broken down (metabolized) in the liver; the main breakdown product is excreted in the urine, with about 75% of the dose eliminated in the first day. The elimination half-life — the time it takes the body to clear half the drug — is roughly 75 minutes in healthy adults. In patients with liver disease (cirrhosis), both the volume of distribution and the half-life are approximately doubled, meaning the drug stays active longer. Older adults also clear etomidate more slowly than younger adults.

How to store Etomidate

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Store at 20 to 25°C (68 to 77°F).

Written from the FDA-approved label with AI and reviewed by our pharmacy team. How we use AI →

5

Supplements & herbs that interact with Etomidate

5 supplements and herbal products have documented interactions with Etomidate in the licensed clinical database we use. Most are manageable — but your pharmacist should know about everything you take, including vitamins and herbals.

Severity mix
  • Major · 1
  • Moderate · 4
Every supplement checked against Etomidate — ranked by severity The full interaction hub: 1 major · 4 moderate · every one linked to its full report. Check Etomidate against your exact supplements

Educational information from a licensed clinical database (Natural Medicines) — see our data sources & update cadence. Not medical advice: an interaction being documented does not mean it will happen to you; do not start or stop medications or supplements without professional guidance.

Etomidate: pharmacist answers to common questions

Quick, plain-English answers to the questions patients ask most about Etomidate — the kind of thing our pharmacy team would talk through with you at the counter.

What exactly is etomidate, and why did my doctor choose it for my procedure?

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Etomidate is a fast-acting anesthetic given through an IV to put you into a deep sleep before surgery or another procedure. One of its biggest advantages is that it has very little effect on your heart and blood pressure compared to some other anesthetics. Your doctor may have chosen it because of your cardiovascular health or because your procedure is short and a quick, stable induction was the priority.

Will I feel anything during the injection, and what should I expect right after?

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Some people notice a brief burning or pain sensation in the vein where the IV is placed — this is common and usually mild. You may also experience some involuntary muscle twitching right as you're going under; this is a well-known effect of etomidate and your care team is prepared for it. Recovery is generally fairly quick, and nausea or vomiting after the procedure is possible, especially with certain types of short surgeries.

I heard this drug affects your stress hormones — should I be worried?

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Etomidate does temporarily lower your body's levels of cortisol and aldosterone — hormones your adrenal glands make to help you handle stress — for roughly 6 to 8 hours after the injection. For a single, short use during anesthesia, this is generally managed by your care team. What's important to know is that etomidate should never be given as a continuous drip over a long period, precisely because of this hormonal effect. If you have any concerns after your procedure — like feeling unusually weak — let your care team know.

Is etomidate safe for children?

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Etomidate is not recommended for children under the age of 10 for inducing anesthesia, because there isn't enough safety data for that age group. For children who do receive any general anesthetic, there is a broader concern across all anesthetic drugs about potential effects on the developing brain — especially in children under about age 3 or during procedures lasting more than 3 hours. If your child needs an elective procedure, it's worth having an honest conversation with their doctor about the timing and necessity.

I'm older and have high blood pressure — is etomidate safe for me?

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Etomidate is actually one of the anesthetics considered when patients have heart or blood pressure concerns, because it tends to have a more stable effect on circulation than some alternatives. That said, older adults — particularly those with high blood pressure — can experience drops in heart rate, blood pressure, and heart output with etomidate. Your anesthesia team will be monitoring you closely throughout, and doses are typically adjusted for older patients.

What should I tell my care team before I receive etomidate?

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Be sure to mention any history of allergic reactions to etomidate or other anesthetics, any liver problems (especially cirrhosis), severe blood loss or trauma, and all medications you take — including fentanyl or other pain medicines that might be used alongside it. If you're pregnant or have a young child receiving anesthesia, make sure to discuss that too. The more your anesthesia team knows, the safer they can make your experience.

Is Etomidate available over the counter?

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No. Etomidate is a prescription medicine: every Etomidate product listed with the FDA is prescription only, so it is not sold over the counter. Your prescriber decides whether it is appropriate for you, and your pharmacist dispenses it.

When was Etomidate first available?

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The earliest FDA record we hold for Etomidate is from 1982: its first approval in Drugs@FDA or its earliest product listing in the NDC Directory, whichever is older. Many older medicines were in use before their first formal FDA approval, so this is the earliest date on record, not necessarily when Etomidate was first used.

Who makes Etomidate?

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12 companies currently list Etomidate products in the FDA's NDC Directory, including Hikma Pharmaceuticals USA Inc., Armas Pharmaceuticals Inc., Caplin Steriles Limited. That count includes repackagers and distributors as well as manufacturers (companies that sell only the raw ingredient are not counted), so fewer companies actually make it; the label on your bottle names the one that supplied yours.

Answers drafted from the FDA-approved label with AI and reviewed by our pharmacy team. How we use AI →

More about Etomidate on HelloPharmacist

Detailed data & references for Etomidate Forms & strengths, pricing, billing codes, manufacturers, safety reports and sourcing — the data behind the page. Most people can stop here. Each section below opens on a tap.

Etomidate forms and strengths (how it comes)

Etomidate is available in 1 form. Different forms and brands can have different approved uses, doses, schedules, and directions. Follow the instructions for your exact product, and do not switch forms without guidance from your prescriber or pharmacist.

Injection

Into a vein
Brands Amidate
How this form is used
What it may be used for
  • Amidate is used intravenously to induce (start) general anesthesia in adults and children over age 10
  • Amidate is used intravenously to supplement weaker anesthetic agents such as nitrous oxide during short procedures like dilation and curettage or cervical conization in adult patients
  • Etomidate injection is used intravenously to induce general anesthesia in adults and children over age 10
  • Etomidate injection is used intravenously to supplement weaker anesthetic agents during short operative procedures in adult patients
Important instructions
  • Amidate and Etomidate injection are given only by intravenous injection by trained anesthesia professionals — never by prolonged continuous infusion
  • The solution should be inspected before use; do not administer if it is not clear or if the container is damaged, and discard any unused portion
  • Amidate dosing is individualized and injected slowly; older adults may require a reduced dose
  • Other anesthetic or neuroactive drugs used alongside Amidate or Etomidate may affect the required dose — the full medication list must be reviewed by the care team
Available strengths 3 strengths
50 FDA-listed product records ⓘ

Etomidate on the U.S. market: products, makers and brands

How Etomidate appears in the FDA’s National Drug Code Directory — including its dosage forms, strengths, brand names, manufacturers, and FDA-listed product records. These are directory records, not sales or prescription volume.

12 companies list 24 Etomidate product records with the FDA, mostly as injection; the earliest marketing or approval year on record is 1982. Brand names on the directory include Amidate; the rest are generics.

1
Dose forms ⓘ
12
Labelers (makers, repackagers, distributors)
2
Brand names
24
FDA-listed product records ⓘ
1982
Earliest FDA record ⓘ

Also listed with the FDA, not a patient dose form: Powder (3) — bulk drug substance sold to compounders/manufacturers and multi-item kits. These aren’t counted in the dose-form total above.

Hikma Pharmaceuticals USA Inc.17%
Armas Pharmaceuticals Inc.8%
Caplin Steriles Limited8%
Civica, Inc.8%
Eugia US LLC8%
Fosun Pharma USA Inc8%
Other makers42%

Share of FDA-listed product records by manufacturer — FDA National Drug Code Directory. Record counts are not sales or prescription volume.

How widely Etomidate is used (Medicaid data)

A general measure of how commonly Etomidate is prescribed, based on Medicaid — one of the largest public drug programs. The figure below is prescriptions filled in Q1–Q4 2025, summed across every form and brand of the drug.

Think of this as a proxy for how widely Etomidate is used, drawn from freely available public data. Medicaid is just one program — these numbers don’t include Medicare, other government coverage, or commercial and cash-pay prescriptions, so real-world use is higher than what’s shown here.

858
Medicaid prescriptions filled (Q1–Q4 2025)
$60,636 gross Medicaid reimbursement (before mandatory rebates — net cost is lower)

How commonly is Etomidate prescribed? Of the 1,601 medications we measure, Etomidate ranks #1,304 by Medicaid prescriptions — more than 19% of them.

Where Etomidate ranks among the drugs we measure · Q1–Q4 2025 · neighbors ±5

Utilization by Etomidate product

Pick a product to see its own Medicaid numbers. Each chip is one clinical product — a specific strength & dosage form as defined by RxNorm — with brand-name and generic versions combined.

The 10 mL / 2 mg/mL injection is the most-dispensed Etomidate product — about 78% of these Medicaid prescriptions.

10 ML etomidate 2 MG/ML Injection Most dispensed

669 Medicaid prescriptions (Q1–Q4 2025) 78% of Etomidate prescriptions shown $40,101 gross reimbursement (before rebates) ≈ $60 per prescription (gross)

Summed across the 6 of 33 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 1654006

20 ML etomidate 2 MG/ML Injection

189 Medicaid prescriptions (Q1–Q4 2025) 22% of Etomidate prescriptions shown $20,535 gross reimbursement (before rebates) ≈ $109 per prescription (gross)

Summed across the 3 of 28 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 1654008

Shares are of the Medicaid prescriptions shown here. Product grouping follows RxNorm (the National Library of Medicine’s drug terminology), so “one product” means one strength & dosage form regardless of manufacturer. Dollar figures are gross Medicaid reimbursement before mandatory rebates — rebates (often large, especially for brand-name drugs) are confidential, so actual net cost to Medicaid is lower than shown.

Source: Medicaid State Drug Utilization Data (CMS), aggregated by generic ingredient — summed across every NDC (all brands, strengths, salt forms and dosage forms) of Etomidate, and across all states and both fee-for-service and managed-care claims. A general popularity signal; it excludes Medicare, commercial insurance and cash prescriptions, so it is not total U.S. use. Based on the 9 of 61 listed Etomidate NDCs with Medicaid activity.

Compare Etomidate products

A representative set of FDA-listed product records for Etomidate — across manufacturers, strengths, and dosage forms, grouped by form with each product’s manufacturer and how the FDA approved it. The same medicine may be made and packaged by different companies, so a single drug can have many directory entries. (It’s also why a refill can look different — a new shape, color, or box — even though it contains the same medication.)

Showing 24 of 24 products — FDA National Drug Code Directory. See every product, package size and price: browse all 24 Etomidate NDCs →

Etomidate recall history

A recall is when a specific batch of a medicine is pulled from the market — usually a manufacturing issue, not a problem with the drug itself. Class I is most serious, Class III least.

The FDA’s enforcement reports list no Etomidate recalls since July 2021.

✅No Etomidate recalls on record since July 2021

Source: FDA enforcement (recall) reports, via openFDA; our copy was last updated Sep 24, 2026.

RxNorm Concept Web — From Ingredient to Every Form and Strength

This page starts with one ingredient concept (IN). The branches below show its dose-form concepts (SCDF), then the available clinical drug and strength concepts (SCD). Combination products remain separate concepts with their own pages.

Ingredient (IN) Etomidate RxCUI 4177 1 dose form · 2 strengths

Look up RxCUI 4177 in the RxCUI Atlas →

RxNorm is the U.S. National Library of Medicine’s normalized drug vocabulary. Its concept hierarchy can include forms that are not currently marketed; the status on each branch compares that concept with current FDA listings. RxCUIs identify vocabulary concepts, not individual packages or manufacturers.

Etomidate brand names

Etomidate is sold under one brand name in the FDA directory — Amidate. A brand and its generic contain the same active ingredient; the brand name belongs to one company's product.

Amidate

Who makes Etomidate: manufacturers and labelers

12 companies list Etomidate products with the FDA. By number of product records, the largest are Hikma Pharmaceuticals USA Inc., Armas Pharmaceuticals Inc., Caplin Steriles Limited. Labelers include manufacturers and repackagers; the product in your bottle depends on which one your pharmacy stocks.

Hikma Pharmaceuticals USA Inc. 4 Armas Pharmaceuticals Inc. 2 Caplin Steriles Limited 2 Civica, Inc. 2 Eugia US LLC 2 Fosun Pharma USA Inc 2 Fresenius Kabi USA, LLC 2 Gland Pharma Limited 2 HF Acquisition Co LLC, DBA HealthFirst 2 Mylan Institutional LLC 2 Henry Schein, Inc. 1 Hospira, Inc. 1

Etomidate drug class (RxNorm)

Etomidate belongs to the General Anesthetic class.

Pharmacologic class General Anesthetic
Drug family (ATC) Other general anesthetics

Classified by RxNorm RxClass — the U.S. National Library of Medicine's standardized drug-classification service (Established Pharmacologic Class from the FDA, the ATC drug family from the WHO, and mechanism of action). Reference only, not medical advice.

Sources for this Etomidate page

Core label, product, RxNorm, safety, and utilization data on this page come from the sources identified below. AI-written, editorial, and licensed sections are labeled separately.

📄
FDA-filed drug labels (SPL) Uses, dosing, warnings & side effects from SPL records retrieved through openFDA; the linked representative set can be verified on DailyMed. ✓ Linked label effective May 20, 2026
🏭
Forms, brands & labelersAggregated from ingredient-matched FDA National Drug Code Directory product records for Etomidate.
📈
Real-world reportsThe FDA Adverse Event Reporting System (FAERS), served through openFDA.
🚨
Recalls & shortagesopenFDA drug-enforcement reports and the FDA drug-shortage database.
🧾 Clinical label set — FDA-filed SPL labels retained for Etomidate after exact ingredient or ingredient-combination matching and applicable route/form matching
Clinical labels in scope
14
Finished products in the current FDA directory
24
Companies listing them (makers, repackagers, distributors)
12
FDA labeler codes behind them ⓘ
12
Linked representative label ⓘ
Hospira, Inc.
Linked label effective
May 20, 2026
Composite sections available
15
Linked SPL Set ID
b7ed5bf8-ba75-44dc-8f81-96b4ad5766be
Linked SPL Document ID
3f83ed21-1b60-486c-8c70-1d5aa7553404
Open the linked representative label on DailyMed ↗

How this page is built

HelloPharmacist combines public FDA and NLM records and does not author the underlying clinical facts. The plain-language sections are written with AI from the FDA-approved label text and reviewed by our pharmacy team before publication. Hospira, Inc. is the representative DailyMed label linked for verification and dates. This is general education, not medical advice: always talk to your doctor or pharmacist about your own medicines. How we build and review drug pages →