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Temazepam: uses, dosing, side effects & brands

Temazepam is a benzodiazepine sold in the U.S. under one brand, for depressive disorder, sleep initiation and maintenance disorders and panic disorder. Below: what the FDA label says, every product that contains it, what the pills look like, and its recall record.

By the pharmaranks editorial teamReviewed against the FDA (openFDA label, NDC Directory & Enforcement) sourcesUpdated Jul 24, 2026How we research

Key facts

Drug class
Benzodiazepine
Treats
Depressive Disorder, Sleep Initiation and Maintenance Disorders and Panic Disorder
Available as
Capsule
Sold as
Temazepam
Prescription?
Prescription only
Generic available?
Yes
What the pharmacy pays
about $3 for a 30-count supply — not your price
Boxed warning
Boxed warning

How temazepam is dosed

From the FDA label for Temazepam (application ANDA201781). Other temazepam products — different forms, different strengths — are dosed differently. Follow the label for the one you were prescribed.

While the recommended usual adult dose is 15 mg before retiring, 7.5 mg may be sufficient for some patients, and others may need 30 mg. In transient insomnia, a 7.5 mg dose may be sufficient to improve sleep latency. In elderly or debilitated patients, it is recommended that therapy be initiated with 7.5 mg until individual responses are determined. Discontinuation or Dosage Reduction of Temazepam Capsules To reduce the risk of withdrawal reactions, use a gradual taper to discontinue temazepam capsules or reduce the dosage. If a patient develops withdrawal reactions, consider pausing the taper or increasing the dosage to the previous tapered dosage level. Subsequently decrease the dosage more slowly ( see WARNINGS, Dependence and Withdrawal Reactions and DRUG ABUSE AND DEPENDENCE: Dependence ).

Temazepam side effects

During controlled clinical studies in which 1,076 patients received temazepam at bedtime, the drug was well tolerated. Side effects were usually mild and transient. Adverse reactions occurring in 1% or more of patients are presented in the following table: Temazepam % Incidence (n=1,076) Placebo % Incidence (n=783) Drowsiness 9.1 5.6 Headache 8.5 9.1 Fatigue 4.8 4.7 Nervousness 4.6 8.2 Lethargy 4.5 3.4 Dizziness 4.5 3.3 Nausea 3.1 3.8 Hangover 2.5 1.1 Anxiety 2.0 1.5 Depression 1.7 1.8 Dry Mouth 1.7 2.2 Diarrhea 1.7 1.1 Abdominal Discomfort 1.5 1.9 Euphoria 1.5 0.4 Weakness 1.4 0.9 Confusion 1.3 0.5 Blurred Vision 1.3 1.3 Nightmares 1.2 1.7 Vertigo 1.2 0.8 The following adverse events have been reported less frequently (0.5% to 0.9%): Central Nervous System – anorexia, ataxia, equilibrium loss, tremor, increased dreaming Cardiovascular – dyspnea, palpitations Gastrointestinal – vomiting Musculoskeletal – backache Special Senses – hyperhidrosis, burning eyes Amnesia, hallucinations, horizontal nystagmus, and paradoxical reactions including restlessness, overstimulation and agitation were rare (less than 0.5%). To report SUSPECTED ADVERSE REACTIONS, contact Solco Healthcare US, LLC at 1-866-257-2597 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.

Temazepam drug interactions

The concomitant use of benzodiazepines and opioids increases the risk of respiratory depression because of actions at different receptor sites in the CNS that control respiration. Benzodiazepines interact at GABAA sites and opioids interact primarily at mu receptors. When benzodiazepines and opioids are combined, the potential for benzodiazepines to significantly worsen opioid-related respiratory depression exists. Limit dosage and duration of concomitant use of benzodiazepines and opioids, and monitor patients closely for respiratory depression and sedation. The benzodiazepines, including temazepam, produce additive CNS-depressant effects when co-administered with other CNS depressants such as alcohol, barbiturates, antipsychotics, sedative/hypnotics, anxiolytics, antidepressants, narcotic analgesics, sedative antihistamines, anticonvulsants, and anesthetics. The pharmacokinetic profile of temazepam does not appear to be altered by orally administered cimetidine dosed according to labeling.

Every temazepam product we track (1)

Same active ingredient — different manufacturer, form, price and FDA recall record. That last one is what our independent score measures.

Only one: Temazepam.

What temazepam pills look like

Imprint codes, colour and shape from the FDA’s labelling data. Match the imprint on your pill — or search any imprint.

Temazepam pill imprints
ImprintStrengthColourShape
FOR;SLEEP;M;RESTORIL;7;5;mg7.5 mgpink, bluecapsule
FOR;SLEEP;M;RESTORIL;15;mg15 mgpink, redcapsule
FOR;SLEEP;M;RESTORIL;22;5;mg22.5 mgbluecapsule
FOR;SLEEP;M;RESTORIL;30;mg30 mgblue, redcapsule
FOR;SLEEP;M;7;5;mg7.5 mgpink, bluecapsule
FOR;SLEEP;M;22;5;mg22.5 mgbluecapsule
FOR;SLEEP;M;15;mg15 mgred, pinkcapsule
FOR;SLEEP;M;30;mg30 mgred, bluecapsule
R;07615 mgwhite, greencapsule
AMNEAL;5837.5 mgwhite, bluecapsule
AMNEAL;55615 mgwhite, bluecapsule
AMNEAL;58422.5 mgwhite, pinkcapsule

How long temazepam keeps

No temazepam label we read sets a separate limit for after opening, but they do specify how it must be stored — and the stability behind any date assumes those conditions.

Does temazepam expire? The in-use limits and storage rules from its labels

Temazepam and breastfeeding

From LactMed, the US National Library of Medicine’s Drugs and Lactation Database — quoted, not rewritten.

Because of the low levels of temazepam in breastmilk and its relatively short half-life, amounts ingested by the infant are small and would not be expected to cause any adverse effects in breastfed infants. Taking the bedtime dose after the infant's last feeding of the day may minimize the dose received by an older infant who is sleeping through the night. Monitor the infant for sedation, poor feeding and poor weight gain.

Full LactMed record for temazepam: levels in milk, effects in breastfed infants, and the drugs it would consider instead

National Institute of Child Health and Human Development, record revised September 15, 2024. LactMed states its information is not a substitute for professional judgement.

What people report to the FDA about temazepam

The FDA Adverse Event Reporting System (FAERS) collects reports from patients and clinicians. It holds 31,190 reports naming temazepam, and the FDA flagged 77% of those reports as serious. The effects reported most often — leaving out reports about overdose, misuse or the condition being treated, which dominate the raw list for common medicines:

  • fatigue2,245 reports
  • nausea1,832 reports
  • headache1,782 reports
  • diarrhoea1,427 reports
  • dyspnoea1,413 reports
  • dizziness1,345 reports
  • fall1,320 reports
  • insomnia1,286 reports

Read these as a signal, not a rate. A report does not mean temazepam caused the effect — anyone can file one, and many describe people taking several medicines for several conditions. Crucially there is no denominator: FAERS does not record how many people took the drug, so these counts cannot be turned into “X% of patients” — a bigger number often just means a more widely used or more talked-about drug. Duplicates exist, and publicity drives reporting. For what is actually established, read the FDA label section above.

Source: openFDA drug/event (FAERS), retrieved July 26, 2026.

Related calculators

Frequently asked questions

What is temazepam?

Temazepam is a benzodiazepine used to treat Depressive Disorder, Sleep Initiation and Maintenance Disorders, Panic Disorder.

What kind of drug is temazepam?

The FDA classifies temazepam as a benzodiazepine. Benzodiazepines boost the brain's main calming chemical, GABA, by binding to the GABA-A receptor and making its chloride channel open more often. This quiets nerve activity, producing sedation, reduced anxiety, muscle relaxation, and protection against seizures. If you are checking whether it is safe to combine with something else, the class is what matters — two drugs from the same class usually should not be stacked.

Can you take temazepam with other medicines?

It depends on the medicine. We check it against the FDA labels rather than guessing: our interaction checker searches each drug's own label for the other and quotes what it says, naming the section it came from. Run temazepam against whatever else you take — and remember that a label not naming a drug is not the same as that combination being safe.

What forms does temazepam come in?

Across the brands we track, temazepam is currently marketed as capsule, per the FDA's National Drug Code Directory. Each form is dosed differently — follow the label for the exact product you were prescribed.

Is there a generic temazepam?

Yes. Our catalog lists 1 generic temazepam product alongside the brand versions. A generic has the same active ingredient and must meet the FDA's bioequivalence standard; it usually costs less. Ask your pharmacist which one your plan covers.

What are the common side effects of temazepam (Restoril)?

Drowsiness is the standout — 9.1% versus 5.6% on placebo in the trials — along with lethargy (4.5% vs 3.4%), dizziness (4.5% vs 3.3%), and next-day hangover (2.5% vs 1.1%). Headache and fatigue were reported too, but at rates matching or below placebo, so they're weak markers of the drug itself. The one that catches people out is next-morning grogginess and impaired driving, since temazepam is still active for hours after you wake up. The label is specific about how to use it: take the capsule immediately before getting into bed, and only when you can devote a full night to sleep before you need to be alert again. Don't take it after already lying awake for hours — that's how a dose lands too close to morning. Older adults face an added risk of falls and should generally use lower doses.

What are temazepam's boxed warnings?

Three. (1) Combining benzodiazepines with opioids can cause profound sedation, respiratory depression, coma, and death — this covers prescription painkillers like oxycodone and hydrocodone, and also cough syrups containing codeine. (2) Abuse, misuse, and addiction, which can lead to overdose and death; the severe reactions reported with benzodiazepine abuse and misuse include delirium, paranoia, suicidal thoughts and behavior, seizures, coma, and breathing difficulty. (3) Physical dependence and withdrawal, with risk rising the longer you take it and the higher the daily dose. Alcohol and other sedatives compound all three. If a new prescriber offers you an opioid, say out loud that you take temazepam.

Why can't I just stop temazepam when I want to?

Abrupt discontinuation or a rapid dose cut after continued use can precipitate acute withdrawal reactions that are life-threatening — seizures among them. Some people develop a protracted withdrawal syndrome with symptoms lasting weeks to more than twelve months. That's why coming off temazepam is a planned, gradual taper set by your prescriber, not something to attempt over a weekend, and why running out of refills unexpectedly is a problem worth calling about before the last capsule. If you've been taking it nightly for more than a few weeks, book the taper conversation now rather than after you decide you want to stop.

What reactions mean stop the drug and call right away?

Complex sleep behaviors: sleepwalking, sleep-driving, cooking, eating, making phone calls, or having sex while not fully awake, usually with no memory of it afterward. One episode is enough to call your prescriber about stopping — alcohol and other CNS depressants make these more likely. Also call for memory gaps, confusion, hallucinations, agitation, or new or worsening depression and suicidal thoughts. Call 911 for swelling of the face, lips, tongue, or throat, or trouble breathing, which can indicate a severe allergic reaction. And if you are pregnant, might be, or are planning to become pregnant, call the prescriber before your next dose: temazepam capsule labeling contraindicates use in women who are or may become pregnant (Pregnancy Category X), and use late in pregnancy can leave a newborn sedated or in withdrawal. Make that call rather than stopping cold on your own — after regular use, the withdrawal risk above is real.

How long is temazepam actually meant to be taken?

It's approved for short-term treatment of insomnia — generally 7 to 10 days. The label makes a useful point about that limit: failure of insomnia to remit after 7 to 10 days of treatment may indicate a primary psychiatric or medical illness — untreated depression, sleep apnea, pain, restless legs, thyroid disease — that should be evaluated rather than covered with a longer prescription. Its safety and effectiveness beyond about two weeks have not been established. Practical next step if you're past that window: ask about cognitive behavioral therapy for insomnia (CBT-I), which has durable effects that don't fade or require a taper, and use it as the bridge while you and your prescriber plan how to reduce the temazepam.

How long does temazepam (Restoril) stay in your system?

Temazepam is an intermediate-acting benzodiazepine with an elimination half-life of about 8–15 hours (FDA label), so most of a dose clears within roughly 2–3 days. In urine it and its metabolites are commonly detectable for about 1–7 days after use; frequent or higher-dose use pushes toward the longer end. In blood it is usually measurable for about 1–2 days. Windows are approximate and depend on dose, duration of use, age, kidney/liver function, and metabolism. This is general information, not medical or legal advice.

Will temazepam make a benzodiazepine drug test positive?

Yes. Temazepam is a true benzodiazepine and generally shows up on benzodiazepine urine immunoassays, and it is also a metabolite of diazepam, so a temazepam-positive result can appear after diazepam use as well. Confirmatory testing (GC-MS or LC-MS/MS) can distinguish the specific drug. If you take temazepam by prescription, disclose it to the lab or medical review officer so the result is interpreted correctly. Detection depends on the assay's cutoff and your dosing; this is not medical or legal advice.

How long can temazepam be detected in saliva or hair?

In oral fluid (saliva), temazepam is typically detectable for about 1–2 days after a dose, making saliva a shorter-window, more recent-use test. In hair, benzodiazepines including temazepam can be detected for up to about 90 days by specialized LC-MS/MS analysis used mainly in forensic contexts. Both are approximate and affected by dose, frequency, and individual factors. Ranges reflect standard toxicology references (LabCorp, Quest, Mayo); this is educational, not medical or legal advice.

Cite this page
APA
pharmaranks. (2026, July 24). Temazepam: uses, dosing, side effects & brands. https://pharmaranks.com/drugs/temazepam
MLA
“Temazepam: uses, dosing, side effects & brands.” pharmaranks, 24 July 2026, https://pharmaranks.com/drugs/temazepam.

We summarise public FDA and NIH sources — for a clinical claim, cite the primary source we link to as well.

Sources: FDA openFDA drug label, National Drug Code Directory, and Enforcement (recall) database. This page reproduces public FDA data and is not medical advice. Dosing is set by your prescriber.

Read the full FDA label for temazepam on DailyMed (NIH) ↗ — including its boxed warning in full.