Citalopram: uses, dosing, side effects & brands
Citalopram is a serotonin reuptake inhibitor sold in the U.S. under 2 brand and generic names, for alcoholism, dementia and depressive disorder. Below: what the FDA label says, every product that contains it, what the pills look like, and its recall record.
Key facts
- Drug class
- Serotonin Reuptake Inhibitor
- Treats
- Alcoholism, Dementia and Depressive Disorder
- Available as
- Tablet
- Sold as
- 2 products — Celexa and Citalopram Hydrobromide
- Prescription?
- Prescription only
- Generic available?
- Yes
- Half-life
- about 35 hours
- Boxed warning
- Boxed warning
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How citalopram is dosed
From the FDA label for Citalopram Hydrobromide (application ANDA219985). Other citalopram products — different forms, different strengths — are dosed differently. Follow the label for the one you were prescribed.
Do not initiate treatment with citalopram capsules. Use another citalopram product for initial dosage titration or dosages other than 30 mg once daily ( 2.1 ). Administer once daily with or without food ( 2.1 ). Recommended dosage of citalopram capsules is 30 mg once daily ( 2.1 ). Citalopram dosages above 40 mg once daily are not recommended due to the risk of QT prolongation ( 2.1 ). When discontinuing citalopram capsules, reduce dose gradually. Gradual dosage reduction will require use of another citalopram product ( 2.4 , 5.6 ). 2.1 Recommended Dosage Do not initiate treatment with citalopram capsules because the only available dose strength is 30 mg. Use another citalopram product for initial dosage, titration, and dosages other than 30 mg once daily. Refer to Prescribing Information of the other citalopram products for the recommended dosage for those products. Administer citalopram capsules orally, once daily, with or without food. Citalopram should be administered at an initial dose of 20 mg once daily, with an increase to a maximum dose of 40 mg once daily at an interval of no less than one week. Citalopram dosages above 40 mg once daily are not recommended due to the risk of QT prolongation [see Warnings and Precautions (5.2) ] . 2.2 Screen for Bipolar Disorder Prior to Starting Citalopram Capsules Prior to initiating treatment with citalopram capsules or another…
Citalopram side effects
The following adverse reactions are discussed in greater detail in other sections of the labeling: Hypersensitivity reactions [see Contraindications (4) ] Suicidal Thoughts and Behaviors in Adolescent and Young Adults [see Warnings and Precautions (5.1) ] QT-Prolongation and Torsade de Pointes [see Warnings and Precautions (5.2) ] Serotonin Syndrome [see Warnings and Precautions (5.3) ] Increased Risk of Bleeding [see Warnings and Precautions (5.4) ] Activation of Mania or Hypomania [see Warnings and Precautions (5.5) ] Discontinuation Syndrome [see Warnings and Precautions (5.6) ] Seizures [see Warnings and Precautions (5.7) ] Angle Closure Glaucoma [see Warnings and Precautions (5.8) ] Hyponatremia [see Warnings and Precautions (5.9) ] Sexual Dysfunction [see Warnings and Precautions (5.10) ] Most commonly observed adverse reactions (incidence at least twice the incidence of placebo) are: fever, arthalgia, myalgia, anorexia, agitation, yawning, sinusitis, ejaculation disorder (primarily ejaculatory delay), decreased libido, and impotence ( 6.1 ). To report SUSPECTED ADVERSE REACTIONS, contact Aurobindo Pharma USA, Inc. at 1-866-850-2876 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch. 6.1 Clinical Trials Experience Because clinical studies are conducted under widely varying conditions, adverse reaction rates observed in the clinical studies of a drug cannot be directly…
Who shouldn’t take citalopram
Citalopram capsules is contraindicated in patients: taking, or within 14 days of stopping, MAOIs (including MAOIs such as linezolid or intravenous methylene blue) because of an increased risk of serotonin syndrome [see Warnings and Precautions (5.3) , Drug Interactions (7) ] . taking pimozide because of risk of QT prolongation [see Drug Interactions (7) ] . with known hypersensitivity to citalopram or any of the inactive ingredients in citalopram capsules. Reactions have included angioedema and anaphylaxis [see Adverse Reactions (6.2) ]. Concomitant use of monoamine oxidase inhibitors (MAOIs) or use within 14 days of discontinuing an MAOI ( 4 ). Concomitant use of pimozide ( 4 ). Known hypersensitivity to citalopram or any of the inactive ingredients of citalopram capsules ( 4 ).
Citalopram drug interactions
Table 5 presents clinically important drug interactions with citalopram capsules. Table 5: Clinically Important Drug Interactions with Citalopram Capsules Monoamine Oxidase Inhibitors (MAOIs) Clinical Impact: Concomitant use of SSRIs, including citalopram capsules, and MAOIs increases the risk of serotonin syndrome. Intervention: Citalopram capsules is contraindicated in patients taking MAOIs, including MAOIs such as linezolid or intravenous methylene blue [see Dosage and Administration (2.3) , Contraindications (4) , Warnings and Precautions (5.3) ] . Pimozide Clinical Impact: Concomitant use of citalopram with pimozide increases plasma concentrations of pimozide, a drug with a narrow therapeutic index, and may increase the risk of QT prolongation and/or ventricular arrhythmias compared to use of citalopram alone [see Clinical Pharmacology (12.3) ]. Intervention: Citalopram capsules is contraindicated in patients taking pimozide [see Contraindications (4) , Warnings and Precautions (5.2) ]. Drugs that Prolong the QTc Interval Clinical Impact: Concomitant use of citalopram with drugs that prolong QT can cause additional QT prolongation compared to the use of citalopram alone [see Clinical Pharmacology (12.3) ]. Intervention: Avoid concomitant use of citalopram capsules with drugs that prolong the QT interval (citalopram capsules is contraindicated in patients taking pimozide) [see Contraindications (4) , Warnings and Precautions (5.2) ]. CYP2C19 Inhibitors Clinical Impact: Concomitant use of citalopram with CYP2C19 inhibitors increases the risk of QT prolongation and/or ventricular arrhythmias compared to the use of citalopram alone [see Clinical Pharmacology (12.3) ]. Intervention: Avoid concomitant use of citalopram capsules with CYP2C19 inhibitors [see Warnings and Precautions (5.2) ]. Other Serotonergic Drugs Clinical Impact: Concomitant use of citalopram capsules with other serotonergic drugs (including other SSRIs, SNRIs, triptans, tricyclic antidepressants, opioids, lithium, buspirone, amphetamines, tryptophan, and St. John's Wort) increases the risk of serotonin syndrome. Intervention: Monitor patients for signs and symptoms of serotonin syndrome, particularly during citalopram capsules initiation and changes in citalopram dosage. If serotonin syndrome occurs, consider discontinuation of citalopram capsules and/or concomitant serotonergic drugs [see Dosage and Administration (2.1 , 2.4 ), Warnings and Precautions (5.3) ]. Drugs That Interfere With Hemostasis (antiplatelet agents and anticoagulants) Clinical Impact: Concomitant use of citalopram and an antiplatelet or anticoagulant may potentiate the risk of bleeding. Intervention: Inform patients of the increased risk of bleeding associated with the concomitant use of citalopram capsules and antiplatelet agents and anticoagulants. For patients taking warfarin, carefully monitor the international normalized ratio [see Warnings and Precautions (5.4) ]. CYP2C19 inhibitors and CYP2C19 poor metabolizers: Avoid concomitant use. There is an increased risk of QT prolongation with concomitant use ( 7 ).
Every citalopram product we track (2)
Same active ingredient — different manufacturer, form, price and FDA recall record. That last one is what our independent score measures.
| # | Drug | Rating | Type | Form | Generic? | Pharmacy pays | |
|---|---|---|---|---|---|---|---|
| 1 | 70/100 | Prescription | Tablet | No data | — | View → | |
| 2 | 68/100 | Prescription | Tablet | No data | — | View → |
What citalopram pills look like
Imprint codes, colour and shape from the FDA’s labelling data. Match the imprint on your pill — or search any imprint.
| Imprint | Strength | Colour | Shape | Maker |
|---|---|---|---|---|
| A;0;6 | 20 mg | pink | capsule | — |
| IG;207 | 20 mg | pink | round | — |
| IG;208 | 40 mg | white | round | — |
| 10 | 10 mg | brown | round | — |
| 2;0;1010 | 20 mg | brown | oval | — |
| A;05 | 10 mg | orange | round | — |
| 4;0;1011 | 40 mg | brown | oval | — |
| 2;0;1010 | 20 mg | brown | oval | — |
| 4;0;1011 | 40 mg | brown | oval | — |
| 2;0;1010 | 20 mg | brown | oval | — |
| 10 | 10 mg | brown | round | — |
| 4;0;1011 | 40 mg | brown | oval | — |
How long does citalopram take to work?
“It may take several weeks before you notice the full benefit of citalopram.” — MedlinePlus, U.S. National Library of Medicine.
What the NIH says about how quickly citalopram worksHow long citalopram keeps
No citalopram 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 citalopram expire? The in-use limits and storage rules from its labelsCitalopram and breastfeeding
From LactMed, the US National Library of Medicine’s Drugs and Lactation Database — quoted, not rewritten.
Full LactMed record for citalopram: levels in milk, effects in breastfed infants, and the drugs it would consider insteadInfants receive citalopram in breastmilk, and it is detectable in low levels in the serum of some. The dosage that the infant receives and serum level achieved are probably related to the genetic metabolic capacity of the mother and infant. A few cases of minor behavioral side effects such as drowsiness or fussiness have been reported, but no adverse effects on development have been found in infants followed for up to 5 years. Infants exposed in utero can have withdrawal effects postpartum despite breastfeeding and continued maternal citalopram use. If citalopram is required by the mother, it is not a reason to discontinue breastfeeding. Some experts do not recommend citalopram during nursing, but a safety scoring system finds citalopram to be acceptable during breastfeeding. If the mother was taking citalopram during pregnancy or if other antidepressants have been ineffective, most experts recommend against changing medications during breastfeeding. Otherwise, agents with lower excretion into breastmilk may be preferred, especially while nursing a newborn or preterm infant. Monitor the infant for excess drowsiness, restlessness, irritability, poor feeding and poor weight gain, especially in younger, exclusively breastfed infants and when using combinations of psychotropic drugs.
National Institute of Child Health and Human Development, record revised June 15, 2026. LactMed states its information is not a substitute for professional judgement.
What people report to the FDA about citalopram
The FDA Adverse Event Reporting System (FAERS) collects reports from patients and clinicians. It holds 26,633 reports naming citalopram, and the FDA flagged 85% 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:
- fatigue1,858 reports
- headache1,690 reports
- nausea1,528 reports
- dizziness1,204 reports
- fall1,193 reports
- anxiety1,145 reports
- diarrhoea1,128 reports
- depression1,092 reports
Read these as a signal, not a rate. A report does not mean citalopram 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 August 25, 2026.
How long citalopram stays in your system
The elimination half-life of citalopram is about 35 hours. The half-life runs longer in some people — roughly 30-50% longer in older adults and about doubled with reduced liver function; citalopram's metabolites are at least 8 times less potent and are not a longer-acting concern.
CELEXA (citalopram hydrobromide) tablet — DailyMed label ↗Half-life is how long the body takes to clear half a dose. It is not the same as how long a drug test can detect it, and it varies with age, kidney and liver function.
Stopping citalopram: withdrawal & how to come off
The label describes a Discontinuation Syndrome: adverse reactions can occur when citalopram is stopped, especially if stopped abruptly. Named symptoms include nausea, sweating, dysphoric mood, irritability, agitation, dizziness, sensory disturbances (such as paresthesia and electric-shock sensations), tremor, anxiety, confusion, headache, lethargy, emotional lability, insomnia, hypomania, tinnitus, and seizures. The label directs that the dose be reduced gradually under a prescriber's supervision rather than stopping abruptly, and tells patients not to stop on their own but to discuss any tapering regimen with their healthcare provider. This discontinuation warning is in Warnings and Precautions, not in the boxed warning (the boxed warning concerns suicidal thoughts and behaviors).
This describes what the label says about stopping — not a schedule to follow on your own. Any change to citalopramis your prescriber’s decision; stopping some medicines abruptly is dangerous.
Citalopram tablet label — DailyMed ↗Is citalopram safe during pregnancy?
The label states a known risk
The label says published studies have NOT established an increased risk of major birth defects or miscarriage with citalopram use in pregnancy. However, it does name real risks: use in the month before delivery is linked to a less-than-2-fold increase in postpartum hemorrhage, and third-trimester SSRI exposure carries risks of persistent pulmonary hypertension of the newborn (PPHN, ~1-2 per 1,000 live births) and poor neonatal adaptation (neonates may have respiratory distress, feeding difficulty, jitteriness, and other complications requiring prolonged hospitalization). The label also stresses the risk of untreated depression, noting women who stop antidepressants in pregnancy are more likely to relapse, and directs providers to weigh both. A pregnancy exposure registry for antidepressants exists (1-844-405-6185). Decisions about use or stopping should be made only with the prescriber.
This is what citalopram’s FDA label says — not a recommendation to take or stop it. In pregnancy, that decision is your prescriber’s; do not start or stop a medicine on your own.
Citalopram — DailyMed FDA label (§8.1 Pregnancy; Adverse Reactions, Weight Changes) ↗Does citalopram cause weight gain?
The label reports weight loss
In the label's Weight Changes section, patients treated with citalopram in controlled trials experienced a weight loss of about 0.5 kg compared with no change for placebo patients. The adverse-reaction listing notes both decreased and increased weight as frequent metabolic events, but the controlled-trial finding the label reports is a small mean weight loss versus placebo.
Only what the FDA label reports — many drugs blamed for weight change online have no weight effect in their label, and we say so rather than repeat the folklore.
Citalopram — DailyMed FDA label (§8.1 Pregnancy; Adverse Reactions, Weight Changes) ↗Related guides
Related calculators
Frequently asked questions
What is citalopram?
Citalopram capsules contain citalopram, a selective serotonin reuptake inhibitor (SSRI).
What kind of drug is citalopram?
The FDA classifies citalopram as a serotonin reuptake inhibitor. Selective serotonin reuptake inhibitors (SSRIs) block the transporter that pulls serotonin back into nerve cells, so more of this mood-related chemical stays in the gaps between neurons to keep signaling. They act mainly on serotonin, which tends to mean fewer side effects than older antidepressants. 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.
Is citalopram safe during pregnancy?
The label says published studies have NOT established an increased risk of major birth defects or miscarriage with citalopram use in pregnancy. However, it does name real risks: use in the month before delivery is linked to a less-than-2-fold increase in postpartum hemorrhage, and third-trimester SSRI exposure carries risks of persistent pulmonary hypertension of the newborn (PPHN, ~1-2 per 1,000 live births) and poor neonatal adaptation (neonates may have respiratory distress, feeding difficulty, jitteriness, and other complications requiring prolonged hospitalization). The label also stresses the risk of untreated depression, noting women who stop antidepressants in pregnancy are more likely to relapse, and directs providers to weigh both. A pregnancy exposure registry for antidepressants exists (1-844-405-6185). Decisions about use or stopping should be made only with the prescriber. This is what citalopram's FDA label says; whether to use it in pregnancy is your prescriber's decision.
Does citalopram cause weight gain?
In the label's Weight Changes section, patients treated with citalopram in controlled trials experienced a weight loss of about 0.5 kg compared with no change for placebo patients. The adverse-reaction listing notes both decreased and increased weight as frequent metabolic events, but the controlled-trial finding the label reports is a small mean weight loss versus placebo.
What happens if you stop taking citalopram?
The label describes a Discontinuation Syndrome: adverse reactions can occur when citalopram is stopped, especially if stopped abruptly. Named symptoms include nausea, sweating, dysphoric mood, irritability, agitation, dizziness, sensory disturbances (such as paresthesia and electric-shock sensations), tremor, anxiety, confusion, headache, lethargy, emotional lability, insomnia, hypomania, tinnitus, and seizures. The label directs that the dose be reduced gradually under a prescriber's supervision rather than stopping abruptly, and tells patients not to stop on their own but to discuss any tapering regimen with their healthcare provider. This discontinuation warning is in Warnings and Precautions, not in the boxed warning (the boxed warning concerns suicidal thoughts and behaviors). Do not stop citalopram on your own — any change is a prescriber-managed decision.
How long does citalopram stay in your system?
The elimination half-life of citalopram is about 35 hours — that is how long the body takes to clear half of a dose. The half-life runs longer in some people — roughly 30-50% longer in older adults and about doubled with reduced liver function; citalopram's metabolites are at least 8 times less potent and are not a longer-acting concern. Half-life is not the same as how long a drug test can detect the drug, and it varies with age, kidney and liver function.
Can you take citalopram 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 citalopram against whatever else you take — and remember that a label not naming a drug is not the same as that combination being safe.
What brand names is citalopram sold under?
We track 2 citalopram-containing products in the U.S.: Celexa and Citalopram Hydrobromide. They are the same active ingredient; they differ in form, manufacturer, price and FDA recall record.
What forms does citalopram come in?
Across the brands we track, citalopram is currently marketed as tablet, 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 citalopram?
Yes. Our catalog lists 1 generic citalopram 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.
How long does it take for citalopram to work?
It works gradually, not overnight. You may notice some early changes — sleep, appetite or energy — within the first 1 to 2 weeks, but the full effect on mood or anxiety usually takes about 4 to 6 weeks (sometimes up to 8). That delay is normal and is why prescribers ask you not to judge it too soon or stop early; give it time and stay in touch about side effects, and never stop abruptly.
What are the common side effects of citalopram, and do they go away?
The most common are nausea, dry mouth, drowsiness, trouble sleeping, increased sweating, and mild tremor. These usually show up in the first week or two and ease as your body adjusts over a few weeks; taking the dose with food helps the nausea. Sexual side effects such as lower desire or delayed orgasm, and small weight changes, are more likely to persist while you keep taking it.
What serious citalopram side effects mean I should call a doctor or get emergency help?
Citalopram has a boxed warning for increased suicidal thoughts and behavior in people under 25, especially in the first weeks or after a dose change, so get help right away for new or worsening depression, agitation, or thoughts of self-harm. It can also prolong the QT interval (a heart-rhythm change), so fainting or a pounding, irregular heartbeat is an emergency. Serotonin syndrome, agitation, fever, fast heartbeat, muscle stiffness or twitching, shivering, or diarrhea, also needs immediate care.
Why is there a dose limit on citalopram?
The FDA limits citalopram to 40 mg a day because higher doses cause more QT-interval prolongation, a heart-rhythm change that can trigger dangerous arrhythmias. The limit drops to 20 mg a day for people over 60, those with liver problems, and those taking certain interacting drugs or who are CYP2C19 poor metabolizers. Do not exceed your prescribed dose.
Which citalopram side effects are normal and which mean stop?
Normal, usually temporary effects are mild nausea, dry mouth, sleepiness or insomnia, and sweating, keep your prescriber informed but you generally don't stop. Call promptly for a fast or irregular heartbeat, fainting, seizures, confusion, or signs of low sodium (headache, weakness, confusion, more common in older adults). Do not stop citalopram abruptly on your own, that can cause dizziness, flu-like feelings, and electric-shock sensations; taper with your doctor.
Cite this page
- APA
- pharmaranks. (2026, July 24). Citalopram: uses, dosing, side effects & brands. https://pharmaranks.com/drugs/citalopram
- MLA
- “Citalopram: uses, dosing, side effects & brands.” pharmaranks, 24 July 2026, https://pharmaranks.com/drugs/citalopram.
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 citalopram on DailyMed (NIH) ↗ — including its boxed warning in full.