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Two medicines, side by side

Latanoprost vs tafluprost

Latanoprost and tafluprost are both labeled for glaucoma. Drugs@FDA records approvals of latanoprost since 1996 and of tafluprost since 2012. Pharmacies paid $1.58 per mL (Latanoprost 0.005% eye drops) and $2.45 per unit (Tafluprost 0.0015% eye drop) (NADAC, October 7, 2026); the strengths differ, so the two prices are not like for like. How each works, in its label's words: Latanoprost, “Latanoprost is a prostaglandin F 2α analogue that is believed to reduce the intraocular pressure (IOP) by increasing the outflow of aqueous humor.”; Tafluprost, “Tafluprost acid, a prostaglandin analog is a selective FP prostanoid receptor agonist which is believed to reduce intraocular pressure by increasing uveoscleral outflow.”

Check it at the source: the latanoprost FDA label on DailyMed (effective December 18, 2025); the tafluprost FDA label on DailyMed (effective April 23, 2026).

Highlights of the latanoprost record

Latanoprost (Xalatan) · label of December 18, 2025

Used for

From the label: indications

XELPROS (latanoprost ophthalmic emulsion) 0.005% is indicated for the reduction of elevated intraocular pressure (IOP) in patients with open-angle glaucoma or ocular hypertension. XELPROS is a prostaglandin F 2α analog indicated for reduction of elevated intraocular pressure in patients with open-angle glaucoma, or ocular hypertension.

On the market

Earliest approval on file
June 5, 1996
Generic labelers
14 labelers
Pharmacy cost
$1.58 per mL

Supply and safety

Shortage
No current entry
Recalls
3

Highlights of the tafluprost record

Tafluprost (Zioptan) · label of April 23, 2026

Used for

From the label: indications

ZIOPTAN® is indicated for reducing elevated intraocular pressure in patients with open-angle glaucoma or ocular hypertension. ZIOPTAN is a prostaglandin analog indicated for reducing elevated intraocular pressure in patients with open-angle glaucoma or ocular hypertension.

On the market

Earliest approval on file
February 10, 2012
Generic labelers
3 labelers
Pharmacy cost
$2.45 per unit

Supply and safety

Shortage
No current entry
Recalls
0

Source: FDA drug labels via openFDA (Latanoprost label of December 18, 2025, Tafluprost label of April 23, 2026); NDC Directory, Drugs@FDA, NADAC, FDA shortages and recalls (October 8, 2026)

How do latanoprost and tafluprost differ on the record?

How each works, in its label's words: Latanoprost, “Latanoprost is a prostaglandin F 2α analogue that is believed to reduce the intraocular pressure (IOP) by increasing the outflow of aqueous humor.”; Tafluprost, “Tafluprost acid, a prostaglandin analog is a selective FP prostanoid receptor agonist which is believed to reduce intraocular pressure by increasing uveoscleral outflow.”

Both are in FDA's class prostaglandin analogs.

Generics: latanoprost since 2011; tafluprost since 2019 (Drugs@FDA).

LatanoprostTafluprost
Labeled forGlaucomaGlaucoma
Pharmacologic classProstaglandin AnalogProstaglandin Analog
How it works (label)Latanoprost is a prostaglandin F 2α analogue that is believed to reduce the intraocular pressure (IOP) by increasing the outflow of aqueous humor.Tafluprost acid, a prostaglandin analog is a selective FP prostanoid receptor agonist which is believed to reduce intraocular pressure by increasing uveoscleral outflow. The exact mechanism of action is unknown at this time.
Half-life (label)n/an/a
Earliest approval on file (Drugs@FDA)June 5, 1996February 10, 2012
First generic approvedMarch 22, 2011August 19, 2019
Generic labelers (NDC)14 labelers3 labelers
Pharmacy cost (NADAC, each one's most listed form; strengths differ)$1.58 per mL (Latanoprost 0.005% eye drops)$2.45 per unit (Tafluprost 0.0015% eye drop)
12-month price change-13%-16%
Boxed warningNoNo
Shortage nowNo current entryNo current entry
Recalls recorded30
FAERS reports (a report is not proof of cause; counts follow how widely a medicine is used)50,6272,906
DEA schedulenonenone

Source: Drugs@FDA, FDA NDC Directory, CMS NADAC of October 7, 2026, FDA shortages and recalls, FAERS via openFDA (FDA files October 8, 2026)

What next?

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