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Olopatadine: uses, dosing, side effects & brands

Olopatadine is a histamine-1 receptor antagonist sold in the U.S. under 3 brand and generic names, for allergic conjunctivitis. 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
Histamine-1 Receptor Antagonist
Treats (across its forms)
Allergic Conjunctivitis
Available as
Spray/Inhaler, metered · Solution · Drops · Spray/Inhaler
Sold as
3 products — Patanase, Olopatadine Hydrochloride and Pataday Once Daily Relief
Prescription?
Both Rx and OTC forms
Generic available?
Yes
What the pharmacy pays
about $1 per gm — not your price

How Pataday Once Daily Relief is dosed

From the FDA label for Pataday Once Daily Relief (application NDA021545). Other olopatadine products — different forms, different strengths — are dosed differently. Follow the label for the one you were prescribed.

Directions adults and children 2 years of age and older: put 1 drop in the affected eye(s) once daily, no more than once per day if using other ophthalmic products while using this product, wait at least 5 minutes between each product replace cap after each use children under 2 years of age: consult a doctor

Every olopatadine product we track (3)

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

Olopatadine products
#DrugRatingPharmacy pays
170/100$1View →
266/100$1View →
3Not yet rated$1View →

Combination products containing olopatadine

A combination is a different drug — different dosing, different warnings. It is listed here so you can find it, not so you can substitute it.

Olopatadine recalls

From the FDA Enforcement database. A recall covers specific lots — not the drug as a whole.

How long olopatadine keeps

The date on a sealed pack is not the only one: some olopatadine labels start a second clock once the product is opened or mixed, as short as 30 days.

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

What people report to the FDA about olopatadine

The FDA Adverse Event Reporting System (FAERS) collects reports from patients and clinicians. It holds 4,254 reports naming olopatadine, and the FDA flagged 36% 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:

  • treatment failure1,934 reports
  • headache134 reports
  • nausea133 reports
  • diarrhoea129 reports
  • pyrexia126 reports
  • rash115 reports
  • fatigue113 reports
  • malaise112 reports

Read these as a signal, not a rate. A report does not mean olopatadine 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 25, 2026.

Related calculators

Frequently asked questions

What is Pataday Once Daily Relief?

Use temporarily relieves itchy eyes due to pollen, ragweed, grass, animal hair and dander

What kind of drug is olopatadine?

The FDA classifies olopatadine as a histamine-1 receptor antagonist. H1 antihistamines work by blocking histamine, the chemical released during an allergic reaction, from attaching to H1 receptors. This prevents the sneezing, itching, runny nose, watery eyes, and hives that histamine would otherwise trigger. 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 olopatadine 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 olopatadine 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 olopatadine sold under?

We track 3 olopatadine-containing products in the U.S.: Patanase, Olopatadine Hydrochloride and Pataday Once Daily Relief. They are the same active ingredient; they differ in form, manufacturer, price and FDA recall record.

What forms does olopatadine come in?

Across the brands we track, olopatadine is currently marketed as spray/inhaler, metered, solution, drops and spray/inhaler, 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 olopatadine?

Yes. Our catalog lists 1 generic olopatadine 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.

Has olopatadine been recalled?

The FDA's Enforcement database lists 2 recall records whose product description mentions olopatadine. The most recent: Olopatadine Hydrochloride Ophthalmic Solution USP 0.1 % (Oct 9, 2025). A recall applies to specific lots, not to the drug as a whole — check the record for the affected lot numbers.

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

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 olopatadine on DailyMed (NIH) ↗.