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Molecule

Oxazepam

Benzodiazepine
Available on requestControlled substancePsychiatry
Presentations
3
Brands
0
Manufacturers
0
Available from stock
0

Oxazepam is a benzodiazepine indicated for the management of anxiety disorders or for the short-term relief of the symptoms of anxiety. It is available as capsules for oral use. MedsAcross supplies Oxazepam 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
Benzodiazepine
ATC classification
N05BA04 Oxazepam · Benzodiazepine drug
US FDA first approval
4 June 1965
EU status
Not recorded
Orphan designation
Not recorded
WHO essential medicine
Not recorded
India (CDSCO)
Not yet confirmed against CDSCO approval lists
Routes
Oral
Dosage forms
Capsule
Identifiers
UNII 6GOW6DWN2ARxCUI 7781CAS 604-75-1DrugBank DB00842Q412299

Clinical information

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

Uses

Oxazepam capsules are indicated for the management of anxiety disorders or for the short-term relief of the symptoms of anxiety. Anxiety or tension associated with the stress of everyday life usually does not require treatment with an anxiolytic. Anxiety associated with depression is also responsive to oxazepam therapy. This product has been found particularly useful in the management of anxiety, tension, agitation and irritability in older patients. Alcoholics with acute tremulousness, inebriation, or with anxiety associated with alcohol withdrawal are responsive to therapy. The effectiveness of oxazepam in long-term use, that is, more than 4 months, has not been assessed by systematic clinical studies. The physician should periodically reassess the usefulness of the drug for the individual patient.

Source: US FDA prescribing information

Dosing overview

Because of the flexibility of this product and the range of emotional disturbances responsive to it, dosage should be individualized for maximum beneficial effects. OXAZEPAM Usual Dose Mild-to-moderate anxiety, with associated tension, irritability, agitation or related symptoms of functional origin or secondary to organic disease 10 to 15 mg, 3 or 4 times daily Severe anxiety syndromes, agitation, or anxiety associated with depression 15 to 30 mg, 3 or 4 times daily Older patients with anxiety, tension, irritability and agitation Initial dosage: 10 mg, 3 times daily. If necessary, increase cautiously to 15 mg, 3 or 4 times daily Alcoholics with acute inebriation, tremulousness, or anxiety on withdrawal 15 to 30 mg, 3 or 4 times daily This product is not indicated in pediatric patients under 6 years of age. Absolute dosage for pediatric patients 6 to 12 years of age is not established.

Source: US FDA prescribing information

Contraindications

History of previous hypersensitivity reaction to oxazepam. Oxazepam is not indicated in psychoses.

Source: US FDA prescribing information

Warnings and precautions

Boxed warning: Concomitant use of benzodiazepines and opioids may result in profound sedation, respiratory depression, coma, and death. • Reserve concomitant prescribing of these drugs for use in patients for whom alternative treatment options are inadequate. • Limit dosages and durations to the minimum required. • Follow patients for signs and symptoms of respiratory depression and sedation. Risks from Concomitant Use with Opioids: Concomitant use of benzodiazepines, including oxazepam, and opioids may result in profound sedation, respiratory depression, coma, and death. Because of these risks, reserve concomitant prescribing of these drugs in patients for whom alternative treatment options are inadequate. Observational studies have demonstrated that concomitant use of opioid analgesics and benzodiazepines increases the risk of drug-related mortality compared to use of opioids alone.

Source: US FDA prescribing information

Side effects

The necessity for discontinuation of therapy due to undesirable effects has been rare. Transient mild drowsiness is commonly seen in the first few days of therapy. If it persists, the dosage should be reduced. In few instances, dizziness, vertigo, headache and rarely syncope have occurred either alone or together with drowsiness. Mild paradoxical reactions, i.e., excitement, stimulation of affect, have been reported in psychiatric patients, these reactions may be secondary to relief of anxiety and usually appear in the first two weeks of therapy. Other side effects occurring during oxazepam therapy include rare instances of minor diffuse skin rashes - morbilliform, urticarial, and maculopapular, nausea, lethargy, edema, slurred speech, tremor, and altered libido. Such side effects have been infrequent and are generally controlled with reduction of dosage.

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 Oxazepam, sorted by availability.

MedicineManufacturerRegisterAvailability
Oxazepam 15 mg capsuleOralGeneric name—US FDAAvailable on request
Oxazepam 10 mg capsuleOralGeneric name—US FDAAvailable on request
Oxazepam 30 mg capsuleOralGeneric name—US FDAAvailable on request

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 4 June 1965Drugs@FDA
EU (EMA)Not recorded—
India (CDSCO)Not yet confirmed against CDSCO approval lists—
United StatesRegisteredUS FDA (NDC directory, openFDA)Checked 12 November 2026

Conditions

Conditions linked to Oxazepam in public data. This is not a list of approved uses, see the clinical information.

Questions and answers

Is Oxazepam available for export from India?

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

Is Oxazepam approved by the US FDA?

Yes. The US FDA first approved Oxazepam on 4 June 1965, according to Drugs@FDA.

Does Oxazepam need cold chain shipping?

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

Which ATC class is Oxazepam in?

Oxazepam is classified under ATC code N05BA04 (Oxazepam).

References

  1. Oxazepam prescribing information (Epic Pharma). U.S. National Library of Medicine, DailyMed. Retrieved 22 September 2025

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