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Bimatoprost

Bimatoprost ophthalmic solution 0.03% is indicated for the reduction of elevated intraocular pressure in patients with open angle glaucoma or ocular h.

Prescription medicine Ophthalmic Safety alerts on record

How to use Bimatoprost

What the official label says. If a doctor prescribed it, follow the prescription. Your pack's leaflet comes first if it is different.

Who it is for

Bimatoprost ophthalmic solution 0.03% is indicated for the reduction of elevated intraocular pressure in patients with open angle glaucoma or ocular hypertension. Bimatoprost ophthalmic solution 0.03% is a prostaglandin analog indicated for the reduction of elevated intraocular pressure in patients with open angle glaucoma or ocular hypertension. ( 1 )

How to take it and how often
  • The recommended dosage is one drop in the affected eye(s) once daily in the evening
  • Bimatoprost ophthalmic solution 0.03% should not be administered more than once daily since it has been shown that more frequent administration of prostaglandin analogs may decrease the intraocular pressure lowering effect
  • Reduction of the intraocular pressure starts approximately 4 hours after the first administration with maximum effect reached within approximately 8 to 12 hours
  • Bimatoprost ophthalmic solution 0.03% may be used concomitantly with other topical ophthalmic drug products to lower intraocular pressure
  • If more than one topical ophthalmic drug is being used, the drugs should be administered at least five minutes apart
  • One drop in the affected eye(s) once daily in the evening
Strengths it comes in

Ophthalmic solution containing bimatoprost 0.3 mg/mL. Ophthalmic solution containing 0.3 mg/mL of bimatoprost. ( 3 )

Children

Use in pediatric patients below the age of 16 years is not recommended because of potential safety concerns related to increased pigmentation following long-term chronic use.

Older adults

No overall clinical differences in safety or effectiveness have been observed between elderly and other adult patients.

While you are taking it
  • Potential for Pigmentation Advise patients about the potential for increased brown pigmentation of the iris, which may be permanent
  • Also inform patients about the possibility of eyelid skin darkening, which may be reversible after discontinuation of bimatoprost ophthalmic solution 0.03%
  • Potential for Eyelash Changes Inform patients of the possibility of eyelash and vellus hair changes in the treated eye during treatment with bimatoprost ophthalmic solution 0.03%
  • These changes may result in a disparity between eyes in length, thickness, pigmentation, number of eyelashes or vellus hairs, and/or direction of eyelash growth. …
Talk to a doctor first if
  • Bimatoprost ophthalmic solution 0.03% is contraindicated in patients with hypersensitivity to bimatoprost or to any of the ingredients [see Adverse Reactions ]
  • Hypersensitivity
Warnings

Pigmentation : Pigmentation of the iris, periorbital tissue (eyelid) and eyelashes can occur. Iris pigmentation is likely to be permanent. ( 5.1 ) Eyelash Changes : Gradual change to eyelashes including increased length, thickness and number of lashes. Usually reversible. ( 5.2 ) 5.1 Pigmentation Bimatoprost ophthalmic solution has been reported to cause changes to pigmented tissues. The most frequently reported changes have been increased pigmentation of the iris, periorbital tissue (eyelid) and eyelashes. Pigmentation is expected to increase as long as bimatoprost is administered. …

Possible side effects

The following adverse reactions are described elsewhere in the labeling: • Pigmentation [see Warnings and Precautions (5.1) ] • Eyelash Changes [see Warnings and Precautions (5.2) ] • Intraocular Inflammation [see Warnings and Precautions (5.3) ] • Macular Edema [see Warnings and Precautions (5.4) ] • Hypersensitivity [see Contraindications (4) ] Most common adverse reaction (45%) is conjunctival hyperemia ( 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 . …

Pregnancy and breastfeeding

8.1 Pregnancy Risk Summary There are no adequate and well-controlled studies of bimatoprost ophthalmic solution 0.03% administration in pregnant women. There is no increase in the risk of major birth defects or miscarriages based on bimatoprost postmarketing experience. …

If you take too much

No information is available on overdosage in humans. If overdose with bimatoprost ophthalmic solution 0.03% occurs, treatment should be symptomatic. In oral (by gavage) mouse and rat general toxicity studies, doses up to 100 mg/kg/day did not produce any toxicity. This dose expressed as mg/m 2 is at least 70 times higher than the accidental dose of one bottle of bimatoprost ophthalmic solution 0.03% for a 10 kg child.

If you miss a dose

Take it when you remember, unless it is nearly time for the next dose. Then skip the missed one. Never take two doses at once to make up for it. Check your leaflet, as some medicines are different.

From the official U.S. FDA label for this active ingredient. Your pack may have a different strength, so always read its leaflet. If a doctor prescribed it, follow the prescription. Ask a pharmacist if you are unsure. Label dated 2023-07-17.

Brands around the world

Products with Bimatoprost as the active ingredient. Names differ between countries.

Registered products

United States (FDA)

BimatoprostBIMATOPROST 1 g/g · Powder · Cayman Pharma s.r.o.
NDC 61556-070Label
BimatoprostBIMATOPROST 1 g/g · Powder · Chirogate International Inc
NDC 68245-0004Label
BimatoprostBIMATOPROST .3 mg/mL · Solution/ Drops · Apotex Corp.
NDC 60505-0583Label
BimatoprostBIMATOPROST 1 kg/kg · Powder · LAURUS LABS LIMITED
NDC 42385-030Label
BimatoprostBIMATOPROST 1 g/g · Powder · LETCO MEDICAL, LLC
NDC 62991-3185Label

Nigeria (NAFDAC)

NAFDACBioptan Eyedrops B4-3909NAFDACGanfort Eye Drops_ A4-101504

Other countries: check your pack's registration number and we point you to your regulator.

Safety alerts and recalls

Bimatoprost powder, Bulk Ingredient, a) 5g (NDC 38779-3066-03), b) 1g (NDC 38779-3066-06), c) 1g (NDC 38779-3066-09) drums, Medisca, Plattsburgh, NYU.S. FDA Class II
31 Mar 2025 · Medisca Inc. · TerminatedCGMP Deviations
Bimatoprost NDC# 82187-1001-1 Container description: The product packed in double self-seal cover and finally packed in Aluminum cover for shipping.U.S. FDA Class II
7 Feb 2025 · Aspen Biopharma Labs Pvt., Ltd. · OngoingCGMP Deviations
Bimatoprost Ophthalmic Solution, 0.03%, For Use in the Eyes Only, Sterile, Rx Only, 7.5 mL bottle, Manufactured by: Lupin Limited, Pithampur (M.P.), INDIA, NDC: 68180-429-03.U.S. FDA Class III
13 Dec 2019 · Lupin Pharmaceuticals Inc. · TerminatedFailed Impurities/Degradation Specifications: Out-of-specification result observed in any other individual impurity.
Bimatoprost Ophthalmic Solution 0.03%, Rx Only, For Topical Application to the Upper Eyelid, Sterile, a) 3 mL bottle NDC 0781-6206-93, b) 5 mL bottle NDC 0781-6206-75, ManufacturedU.S. FDA Class III
17 Oct 2019 · Sandoz Inc · TerminatedLabeling: Incorrect or missing package insert.

A recall usually affects certain batches only. Compare the lot number on your pack.

Check your pack of Bimatoprost

Or take photos of the pack
3 free checks left today Official sources: U.S. FDA · EMA (EU) · NAFDAC · WHO alerts

Questions about Bimatoprost

What is Bimatoprost used for?

Bimatoprost ophthalmic solution 0.03% is indicated for the reduction of elevated intraocular pressure in patients with open angle glaucoma or ocular hypertension. Bimatoprost ophthalmic solution 0.03% is a prostaglandin analog indicated for the reduction of elevated intraocular pressure in patients with open angle glaucoma or ocular hypertension. ( 1 ) (From the official U.S. FDA label.)

How do I take Bimatoprost?

Follow your prescription or the leaflet in your pack. The official label says: The recommended dosage is one drop in the affected eye(s) once daily in the evening. Bimatoprost ophthalmic solution 0.03% should not be administered more than once daily since it has been shown that more frequent administration of prostaglandin analogs may decrease the intraocular pressure lowering effect. Reduction of the intraocular pressure starts approximately 4 hours afte…

Do I need a prescription for Bimatoprost?

Usually yes. Bimatoprost is a prescription medicine in most countries. Rules differ by country.

What brands contain Bimatoprost?

Bimatoprost is sold under names such as Durysta, Zolymbus, Lumigan, Latisse, Bimatoprost. Brand names differ between countries.

How can I check that my Bimatoprost is genuine?

Scan the registration number on your pack with PillVera (NAFDAC number in Nigeria, NDC in the United States, DIN in Canada), check the expiry date and buy only from licensed pharmacies.