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Molecule

Methohexital

Also known as methohexital sodium
Available on requestControlled substancePsychiatryPain and anaesthesia
Presentations
3
Brands
1
Manufacturers
1
Available from stock
0

Methohexital is a barbiturate. It is available as injection and powder for injection for intravenous, intramuscular and rectal use. MedsAcross supplies Methohexital for export from India to licensed hospitals, importers and physicians acting for named patients, with the documents each country requires.

Information from the US FDA prescribing information, retrieved 12 November 2026. Not yet medically reviewed.How we review

Key facts

Pharmacological class
Barbiturate
ATC classification
N01AF01 Methohexital · Anaesthetics, subgroup N01A, subgroup N01AFN05CA15 Methohexital · Hypnotics and sedatives, subgroup N05CA
US FDA first approval
27 June 1960
EU status
Not recorded
Orphan designation
Not recorded
WHO essential medicine
Not recorded
India (CDSCO)
Not yet confirmed against CDSCO approval lists
Routes
Intravenous, Intramuscular, Rectal
Dosage forms
Injection, Powder for injection
Identifiers
UNII E5B8ND5IPERxCUI 6847CAS 151-83-7DrugBank DB00474Q851813

Clinical information

From the regulator-approved product information. Each section names its source.

Uses

BREVITAL can be used in adults as follows: 1. For intravenous induction of anesthesia prior to the use of other general anesthetic agents. 2. For intravenous induction of anesthesia and as an adjunct to subpotent inhalational anesthetic agents (such as nitrous oxide in oxygen) for short surgical procedures, BREVITAL may be given by infusion or intermittent injection. 3. For use along with other parenteral agents, usually narcotic analgesics, to supplement subpotent inhalational anesthetic agents (such as nitrous oxide in oxygen) for longer surgical procedures. 4. As intravenous anesthesia for short surgical, diagnostic, or therapeutic procedures associated with minimal painful stimuli. 5. As an agent for inducing a hypnotic state. BREVITAL can be used in pediatric patients older than 1 month as follows: 1.

Source: US FDA prescribing information

Dosing overview

Facilities for assisting ventilation and administering oxygen are necessary adjuncts for all routes of administration of anesthesia. Since cardiorespiratory arrest may occur, patients should be observed carefully during and after use of BREVITAL. Age- and size- appropriate resuscitative equipment (i.e., intubation and cardioversion equipment, oxygen, suction, and a secure intravenous line) and personnel qualified in its use must be immediately available. Preanesthetic medication is generally advisable. BREVITAL may be used with any of the recognized preanesthetic medications. Preparation of Solution FOLLOW DILUTION INSTRUCTIONS EXACTLY. Freshly prepare solutions of BREVITAL and use promptly. Reconstituted solutions of BREVITAL are chemically stable at room temperature for 24 hours. Diluents ONLY USE BACTERIOSTATIC-FREE DILUENT – Recommended diluents are based on route of administration.

Source: US FDA prescribing information

Contraindications

BREVITAL is contraindicated in patients in whom general anesthesia is contraindicated, in those with latent or manifest porphyria, or in patients with a known hypersensitivity to barbiturates.

Source: US FDA prescribing information

Warnings and precautions

Boxed warning (brevital): should be used only in hospital or ambulatory care settings that provide for continuous monitoring of respiratory (e.g. pulse oximetry) and cardiac function. Immediate availability of resuscitative drugs and age- and size-appropriate equipment for bag/valve/mask ventilation and intubation and personnel trained in their use and skilled in airway management should be assured. As with all potent anesthetic agents and adjuncts, BREVITAL should be used only in hospital or ambulatory care settings that provide for continuous monitoring of respiratory (e.g. pulse oximetry) and cardiac function. Immediate availability of resuscitative drugs and age- and size-appropriate equipment for bag/valve/mask ventilation and intubation and personnel trained in their use and skilled in airway management should be assured.

Source: US FDA prescribing information

Side effects

Side effects associated with BREVITAL are extensions of pharmacologic effects and include: Cardiovascular Circulatory depression, thrombophlebitis, hypotension, tachycardia, peripheral vascular collapse, and convulsions in association with cardiorespiratory arrest Respiratory Respiratory depression (including apnea), cardiorespiratory arrest, laryngospasm, bronchospasm, hiccups, and dyspnea Neurologic Skeletal muscle hyperactivity (twitching), injury to nerves adjacent to injection site, and seizures Psychiatric Emergence delirium, restlessness, and anxiety may occur, especially in the presence of postoperative pain Gastrointestinal Nausea, emesis, abdominal pain, and liver function tests abnormal Allergic Erythema, pruritus, urticaria, and cases of anaphylaxis have been reported rarely Other Other adverse reactions include pain at injection site, salivation, headache, and rhinitis For medical advice about adverse reactions contact your medical professional.

Source: US FDA prescribing information

Interactions

Prior chronic administration of barbiturates or phenytoin (e.g. for seizure disorder) appears to reduce the effectiveness of BREVITAL. Barbiturates may influence the metabolism of other concomitantly used drugs, such as phenytoin, halothane, anticoagulants, corticosteroids, ethyl alcohol, and propylene glycol-containing solutions.

Source: US FDA prescribing information

For healthcare professionals and buyers. This is not medical advice. Treatment decisions belong to the prescriber.

All presentations

3 presentations of Methohexital, sorted by availability.

MedicineManufacturerRegisterAvailability
Brevital Sodium 500 mg powder for injectionIntramuscular, intravenous, rectalPar HealthUS FDAAvailable on request
Methohexital 500 mg/500 mg injectionIntramuscular, intravenous, rectalGeneric name—US FDAAvailable on request
Methohexital 500 mg/500 mg injectionIntravenousGeneric name—US FDAAvailable on request

Brands by market

1 brand names across 1 markets.

Brand names by country

United States

Manufacturers

Regulatory status

Approval facts from US FDA, EMA and CDSCO data, and registration status by country where we hold register data.

RegisterStatusSource
US FDAFirst approved 27 June 1960Drugs@FDA
EU (EMA)Not recorded—
India (CDSCO)Not yet confirmed against CDSCO approval lists—
United StatesRegisteredUS FDA (NDC directory, openFDA)Checked 12 November 2026

Questions and answers

Is Methohexital available for export from India?

Yes, on request. MedsAcross lists 3 presentations of Methohexital and sources them for licensed hospitals, importers and physicians against valid import documents.

What brand names does Methohexital have?

The catalogue lists 1 brand names for Methohexital, including Brevital Sodium.

Is Methohexital approved by the US FDA?

Yes. The US FDA first approved Methohexital on 27 June 1960, according to Drugs@FDA.

Does Methohexital need cold chain shipping?

No listed presentation of Methohexital is recorded as needing a cold chain. Storage conditions are shown on each presentation page.

Which ATC class is Methohexital in?

Methohexital is classified under ATC code N01AF01 (Methohexital).

References

  1. Brevital Sodium prescribing information (Par Health). U.S. National Library of Medicine, DailyMed. Retrieved 5 May 2026

Request Methohexital for export supply

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