Latanoprost Ophthalmic
Latanoprost ophthalmic solution lowers elevated eye pressure in adults with open-angle glaucoma or ocular hypertension.
🧬 Where this information comes from Click to expand
The clinical label records used on this page are FDA-filed Structured Product Labeling (SPL) retrieved through openFDA. We identified 20 clinical label sets within the page’s selected clinical scope after exact ingredient or ingredient-combination matching and applicable route/form matching. Forms, routes, brands, labelers, strengths, and NDC product-record counts are built separately from matching FDA National Drug Code Directory records. The linked DailyMed document is a representative official source for verification, not the page’s only clinical source. View the linked label on DailyMed →
📖 Latanoprost Ophthalmic: Patient Information Guide
A plain-language walkthrough of Latanoprost Ophthalmic — what it treats, how it works, how it’s taken, side effects, warnings and interactions. Tap any section to expand it.
🎯What it's used for▾
Latanoprost ophthalmic solution is used to lower elevated eye pressure in adults. It is approved for:
- Open-angle glaucoma — the most common form of glaucoma, where fluid drainage from the eye is impaired
- Ocular hypertension — elevated pressure inside the eye that can increase the risk of glaucoma and optic nerve damage
⚙️How it works▾
Latanoprost belongs to a class of medications called prostaglandin F2α analogues. It works by increasing the flow of fluid (aqueous humor) out of the eye through a route called the uveoscleral outflow pathway. By improving drainage, it lowers the pressure inside the eye — which helps protect the optic nerve from damage. Elevated eye pressure is one of the leading risk factors for glaucoma-related vision loss.
💊How it's taken▾
Latanoprost ophthalmic solution is applied as eye drops, once each evening. Using it more than once a day is not recommended — it can actually reduce effectiveness or raise eye pressure rather than lower it.
- Apply one drop into the affected eye or eyes each evening
- If you miss a dose, resume with your next scheduled dose — do not apply extra drops to make up for a missed one
- Remove contact lenses before applying drops; you can reinsert them 15 minutes later
- If using Iyuzeh single-use units, open one unit just before use and discard any remaining solution immediately after — do not store opened units
🤒Side effects — in detail▾
The most commonly reported side effects affect the eye and include:
- Foreign body sensation (gritty feeling in the eye)
- Burning or stinging after application
- Blurred vision
- Red or pink eye (conjunctival hyperemia)
- Itching
- Small surface damage to the cornea (punctate keratitis)
- Gradual darkening of iris (eye) color
- Eyelash changes: longer, thicker, darker, or more numerous lashes
- Excessive tearing, eye pain, or eyelid discomfort (less common)
Contact your doctor if you develop eye pain or inflammation, sudden vision changes, or any signs of serious skin or breathing reactions — these can be serious and need prompt evaluation.
⚠️Warnings & precautions▾
- Permanent iris color change: Latanoprost can gradually make the iris (colored part of the eye) more brown. This change is likely permanent — even after stopping the medication. If you notice a change in eye color, tell your doctor but do not stop using the drops without guidance.
- Eyelid and eyelash changes: The skin around the eye may darken, and eyelashes may become longer, thicker, or grow in abnormal directions. These changes are often reversible after stopping the medication.
- Eye inflammation: Use with caution if you have a history of iritis or uveitis (eye inflammation); avoid during active inflammation.
- Macular edema: There is a risk of swelling in the center of the retina, especially in people who have had certain types of eye surgery or lens removal.
- Herpes eye infection: Latanoprost can reactivate herpes simplex keratitis (a viral eye infection). Avoid it during active infection and use caution if you have a prior history.
- Contact lens wearers: This product contains benzalkonium chloride, which can be absorbed by soft contact lenses. Always remove lenses before use and wait 15 minutes before reinserting.
🔀What it interacts with▾
There are a few important interactions to be aware of with latanoprost ophthalmic solution:
- Other prostaglandin eye drops: Using two or more prostaglandin medicines together is not recommended — it can reduce how well they work or even raise eye pressure
- Thimerosal-containing eye drops: Mixing with drops that contain thimerosal (a preservative) can cause a physical reaction (precipitation); use them at least 5 minutes apart
- Other topical eye medications: Allow at least 5 minutes between each eye drop product to prevent dilution or interaction
This is not a complete list of interactions. Always talk with your doctor or pharmacist before starting, stopping, or changing any medication.
📋Before taking it▾
- Do not use if you are allergic to latanoprost, benzalkonium chloride, or any other ingredient in the product
- Tell your doctor if you have a history of eye inflammation (iritis or uveitis) — active inflammation is a reason to avoid this medication
- Tell your doctor if you have ever had a herpes simplex eye infection — latanoprost can trigger a recurrence
- Tell your doctor if you have had cataract surgery, are missing your natural lens (aphakia), or have a damaged lens capsule — risk of macular edema is increased
- Pregnancy: Animal studies showed birth defects and pregnancy loss at high IV doses; no adequate human data exist. Discuss the risks and benefits with your doctor
- Breastfeeding: It is unknown whether latanoprost passes into breast milk; use with caution and discuss with your doctor
- Children: Safety and effectiveness have not been established in pediatric patients
- Older adults: No significant differences in safety or effectiveness compared to younger adults have been observed
🚑If you take too much▾
Accidentally using too many drops is unlikely to cause serious harm based on available data, but if a large amount is ingested or enters the body, symptoms may include abdominal pain, dizziness, fatigue, hot flushes, nausea, and sweating. If you suspect an overdose, contact your doctor or a poison control center and treat symptoms as they arise.
📡Pharmacodynamics — effects in the body▾
Latanoprost begins lowering intraocular pressure (pressure inside the eye) about 3 to 4 hours after it is applied. The maximum pressure-lowering effect is reached 8 to 12 hours after administration. A single evening dose keeps pressure reduced for at least 24 hours, which is why it is dosed just once daily.
🔬Pharmacokinetics — how your body processes it▾
When applied to the eye, latanoprost is absorbed through the cornea, where it is converted from a prodrug (inactive form) into its active form. Peak levels in the fluid inside the eye are reached about 2 hours after application. Any drug that reaches the bloodstream is quickly broken down by the liver, with a half-life in plasma of only about 17 minutes. The breakdown products are primarily eliminated through the urine.
📦How to store it▾
Store unopened bottle under refrigeration at 2° to 8°C (36° to 46°F). stored at room temperature up to 25°C (77°F) for 6 weeks. Protect from light.
📄 Written from Latanoprost Ophthalmic’s FDA-approved label information, summarized in plain language with AI, and reviewed by our pharmacy team before publication. Every point is grounded in that labeling — nothing is invented. How we use AI →
🩺 Pharmacist Counseling Corner
Quick, plain-English answers to the questions patients ask most about Latanoprost Ophthalmic — the kind of thing our pharmacy team would talk through with you at the counter.
Why do I have to use this at night? Can I use it in the morning instead? ▾
Will my eye color really change? Is that permanent? ▾
My eyelashes look longer and thicker. Is that from these drops? ▾
I wear contact lenses — do I need to do anything special? ▾
Can I use other eye drops at the same time as latanoprost? ▾
Is it okay to use during pregnancy or while breastfeeding? ▾
Is Latanoprost Ophthalmic available over the counter? ▾
When was Latanoprost Ophthalmic first available? ▾
Who makes Latanoprost Ophthalmic? ▾
💬 Answers drafted from Latanoprost Ophthalmic’s FDA-approved label information, summarized in plain language with AI, and reviewed by our pharmacy team before publication. Grounded in that labeling — nothing is made up. How we use AI →
🧰 Keep exploring
💊 How Latanoprost Ophthalmic comes
Latanoprost Ophthalmic is available in 1 form. Different forms and brands can have different approved uses, doses, schedules, and directions. Follow the instructions for your exact product, and do not switch forms without guidance from your prescriber or pharmacist.
Eye drops
How this form is used
- Reduces elevated intraocular pressure in adults with open-angle glaucoma
- Reduces elevated intraocular pressure in adults with ocular hypertension
- Iyuzeh: Use one drop in the affected eye(s) once daily in the evening; do not exceed once-daily dosing
- Iyuzeh: Remove contact lenses before applying and wait at least 15 minutes before reinserting them
- Iyuzeh: Each single-use unit should be used immediately after opening and any remaining solution discarded — do not save for later
- If using other eye drops, wait at least 5 minutes between each medication
📊 Latanoprost Ophthalmic across the U.S. market
How Latanoprost Ophthalmic appears in the FDA’s National Drug Code Directory — including its dosage forms, strengths, brand names, manufacturers, and FDA-listed product records. These are directory records, not sales or prescription volume.
Share of FDA-listed product records by manufacturer — FDA National Drug Code Directory. Record counts are not sales or prescription volume.
📈 How widely Latanoprost Ophthalmic is used
A general measure of how commonly Latanoprost Ophthalmic is prescribed, based on Medicaid — one of the largest public drug programs. The figure below is prescriptions filled in Q1–Q4 2025, summed across every form and brand of the drug.
Think of this as a proxy for how widely Latanoprost Ophthalmic is used, drawn from freely available public data. Medicaid is just one program — these numbers don’t include Medicare, other government coverage, or commercial and cash-pay prescriptions, so real-world use is higher than what’s shown here.
How commonly is Latanoprost Ophthalmic prescribed? Of the 1,597 medications we measure, Latanoprost Ophthalmic ranks #190 by Medicaid prescriptions — more than 88% of them.
Utilization by Latanoprost Ophthalmic product
Pick a product to see its own Medicaid numbers. Each chip is one clinical product — a specific strength & dosage form as defined by RxNorm — with brand-name and generic versions combined.
latanoprost 0.05 MG/ML Ophthalmic Solution
Summed across the 11 of 27 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 314072
Shares are of the Medicaid prescriptions shown here. Product grouping follows RxNorm (the National Library of Medicine’s drug terminology), so “one product” means one strength & dosage form regardless of manufacturer. Dollar figures are gross Medicaid reimbursement before mandatory rebates — rebates (often large, especially for brand-name drugs) are confidential, so actual net cost to Medicaid is lower than shown.
Source: Medicaid State Drug Utilization Data (CMS), aggregated by generic ingredient — summed across every NDC (all brands, strengths, salt forms and dosage forms) of Latanoprost Ophthalmic, and across all states and both fee-for-service and managed-care claims. A general popularity signal; it excludes Medicare, commercial insurance and cash prescriptions, so it is not total U.S. use. Based on the 11 of 27 listed Latanoprost Ophthalmic NDCs with Medicaid activity.
🔍 Compare Latanoprost Ophthalmic products
A representative set of FDA-listed product records for Latanoprost Ophthalmic — across manufacturers, strengths, and dosage forms, grouped by form with each product’s manufacturer and how the FDA approved it. The same medicine may be made and packaged by different companies, so a single drug can have many directory entries. (It’s also why a refill can look different — a new shape, color, or box — even though it contains the same medication.)
| Strength | Route | Manufacturer / Labeler | Category ⓘ | Details |
|---|---|---|---|---|
| 💊Eye drops | ||||
| 50 mcg/mL | Ophthalmic | A-S Medication Solutions × 4 listings | ANDA | View NDC → |
| 50 mcg/mL | Ophthalmic | Aurobindo Pharma Limited × 3 listings | ANDA | View NDC → |
| 50 mcg/mL | Ophthalmic | Bausch & Lomb Incorporated × 3 listings | ANDA | View NDC → |
| 50 mcg/mL | Ophthalmic | Direct Rx | ANDA | Find on DailyMed ↗ |
| 50 mcg/mL | Ophthalmic | Gland Pharma Limited | ANDA | View NDC → |
| 50 mcg/mL | Ophthalmic | Glenmark Pharmaceuticals Inc | ANDA | View NDC → |
| 50 mcg/mL | Ophthalmic | Greenstone LLC × 2 listings | NDA AUTHORIZED GENERIC | View NDC → |
| 50 mcg/mL | Ophthalmic | Lifestar Pharma LLC × 2 listings | ANDA | View NDC → |
| 50 mcg/mL | Ophthalmic | Micro Labs Limited | ANDA | View NDC → |
| 50 mcg/mL | Ophthalmic | Mylan Pharmaceuticals Inc. | NDA AUTHORIZED GENERIC | View NDC → |
| 50 mcg/mL | Ophthalmic | NuCare Pharmaceuticals, Inc. | ANDA | View NDC → |
| 50 mcg/mL | Ophthalmic | NuCare Pharmaceuticals,Inc. × 6 listings | ANDA | View NDC → |
| 50 mcg/mL | Ophthalmic | Pfizer Laboratories Div Pfizer Inc × 2 listings | NDA | View NDC → |
| 50 mcg/mL | Ophthalmic | Proficient Rx LP × 2 listings | ANDA | View NDC → |
| 50 mcg/mL | Ophthalmic | Rising Pharmaceuticals, Inc. | ANDA | View NDC → |
| 50 mcg/mL | Ophthalmic | Rising Pharma Holdings, Inc. × 3 listings | ANDA | View NDC → |
| 50 mcg/mL | Ophthalmic | Sagent Pharmaceuticals | ANDA | View NDC → |
| 50 mcg/mL | Ophthalmic | Sandoz Inc × 3 listings | ANDA | View NDC → |
| 50 mcg/mL | Ophthalmic | Somerset Therapeutics, LLC × 3 listings | ANDA | View NDC → |
| 0.05 mg/mL | Ophthalmic, Topical | Sun Pharmaceutical Industries, Inc. | NDA | View NDC → |
| 0.05 mg/mL | Ophthalmic; Topical | Sun Pharmaceutical Industries, Inc. × 2 listings | NDA | View NDC → |
| 50 mcg/mL | Ophthalmic | Thea Pharma Inc. × 2 listings | NDA | View NDC → |
| 50 mcg/mL | Ophthalmic | Viatris Specialty LLC | NDA | View NDC → |
Showing 47 of 47 products — FDA National Drug Code Directory. See every product, package size and price: browse all 47 Latanoprost Ophthalmic NDCs →
📈 What people report — real-world data (FDA FAERS)
After a medicine reaches the market, patients, doctors and drugmakers can send the FDA reports of problems they think may be linked to it. Here’s what’s been reported for Latanoprost Ophthalmic — a signal of what to watch for, not proof the drug caused it.
Source: openFDA, from the FDA Adverse Event Reporting System (FAERS). These are voluntary reports — they don’t prove the drug caused the effect, and counts reflect how often something was reported, not how often it actually happens. Reports also often name the very problem the medicine is taken for — a common reason to file one is that the drug didn’t help — so for a pain reliever you may see “pain” high on the list; that points to why the report was filed, not to the drug causing the symptom. This counts every report that lists Latanoprost Ophthalmic in any role, so the total runs higher than the FDA’s official dashboard, which counts only cases where the drug is the suspect. For the authoritative figures, see the FDA FAERS Public Dashboard. Always talk to your pharmacist or doctor.
🏛️ The road to your pharmacy
How Latanoprost Ophthalmic went from FDA review to the pharmacy shelf — the key milestones in its regulatory journey.
Source: Drugs@FDA.
🚨 Recall history
A recall is when a specific batch of a medicine is pulled from the market — usually a manufacturing issue, not a problem with the drug itself. Class I is most serious, Class III least.
Source: openFDA drug enforcement (recall) reports.
RxNorm Concept Web — From Ingredient to Every Form and Strength
This page starts with one ingredient concept (IN). The branches below show its dose-form concepts (SCDF), then the available clinical drug and strength concepts (SCD). Combination products remain separate concepts with their own pages.
RxCUI 43611 2 dose forms · 2 strengths
-
Dose form (SCDF) Ophthalmic Solution RxCUI 377441In current FDA listingsClinical drug / strength (SCD) 0.05 MG/MLRxCUI 314072 -
Dose form (SCDF) Ophthalmic Suspension RxCUI 2056742In current FDA listingsClinical drug / strength (SCD) 0.05 MG/MLRxCUI 2056743
Look up RxCUI 43611 in the RxCUI Atlas →
RxNorm is the U.S. National Library of Medicine’s normalized drug vocabulary. Its concept hierarchy can include forms that are not currently marketed; the status on each branch compares that concept with current FDA listings. RxCUIs identify vocabulary concepts, not individual packages or manufacturers.
📦 Supply & shortage status
Whether Latanoprost Ophthalmic is in short supply in the U.S. right now, plus any shortage history the FDA has on record. A shortage usually reflects a manufacturing or demand issue — not a safety problem with the drug.
Source: openFDA, from the FDA Drug Shortages database.
🏷️ Sold under these brand names
🏭 Manufacturers & labelers
RxNorm drug class
Latanoprost Ophthalmic belongs to the Prostaglandin Analog class.
Classified by RxNorm RxClass — the U.S. National Library of Medicine's standardized drug-classification service (Established Pharmacologic Class from the FDA, the ATC drug family from the WHO, and mechanism of action). Reference only, not medical advice.
🔬 Where this comes from
Core label, product, RxNorm, safety, and utilization data on this page come from the sources identified below. AI-written, editorial, and licensed sections are labeled separately.
How we combine label and product data
HelloPharmacist combines public FDA and NLM records; we don’t author the underlying clinical facts. We identified 20 FDA-filed SPL label sets within the page’s selected clinical scope after exact ingredient or ingredient-combination matching and applicable route/form matching. The representative label is the starting point for the displayed reference monograph; the 12 largest stored in-scope SPL records, which may include that representative, are compared section by section, and the longest available version of each section is retained. Forms, routes, brands, labelers, product-listed strengths, and product-record counts are aggregated separately from ingredient-matched FDA NDC Directory records; package records listed above are associated with the linked SPL; and the normalized concept hierarchy comes from NLM RxNorm.
Where a section is identified as AI-written, its plain-language text is generated from bounded label evidence. New draft drug pages remain in the admin review queue before first publication. Thea Pharma Inc. is the representative DailyMed label linked for verification and dates; it is not the sole source used for the page.
This is general education, not medical advice — always consult your doctor or pharmacist about your medications and any medical condition. For the exact wording of the linked representative label, view that label on DailyMed; some displayed composite sections may come from other in-scope SPL labels. Learn how we use AI and our data sources & update cadence.