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Bioptan Eyedrops

NAFDAC注册号 B4-3909 药物

已在NAFDAC注册。注册有效As of 29 October 2026 · synced automatically from official sources.
产品
Bioptan Eyedrops
NAFDAC编号
B4-3909
活性成分
Bimatoprost
强度
0.03%
年级
Eye drops
包装规格
1 x 5 mL (in LDPE bottle)
制造商
未上榜
申请人(持有人)
Korlyns Pharmaceuticals Ltd
Approved
26 Apr 2023
Status
Active View on NAFDAC ↗
Registration valid to
25 Apr 2028
WHO提醒
None found
Community reports
None
Times checked
0

About the medicine: Bimatoprost: uses, dosage and brands worldwide

What we found

  • Bioptan Eyedrops is on the NAFDAC register with an active registration (B4-3909). A valid number alone does not prove a pack is genuine — counterfeiters copy real numbers, so also check the expiry date, seal and print quality.

Generated automatically from the NAFDAC register, WHO alerts and community data as of today. This is not medical advice. Always follow your doctor or pharmacist.

How to use Bioptan Eyedrops

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.

Label for bimatoprost, the active ingredient registered with NAFDAC.

Check your pack of Bioptan Eyedrops

Add the expiry date on your pack for a full Trust Score.

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3 free checks left today Official sources: U.S. FDA · EMA (EU) · NAFDAC · WHO alerts

About Bioptan Eyedrops

What is in Bioptan Eyedrops?

Bioptan Eyedrops contains Bimatoprost (0.03%), as eye drops, according to its NAFDAC registration record.

Is Bioptan Eyedrops registered with NAFDAC?

Yes. Bioptan Eyedrops is listed on the NAFDAC register under registration number B4-3909, and its registration is active as of 29 October 2026.

Has Bioptan Eyedrops been flagged as fake or recalled?

No WHO falsified or substandard medical product alert currently matches Bioptan Eyedrops in our automatically synced alert list.

How can I check that my pack of Bioptan Eyedrops is genuine?

Run a free authenticity scan with the NAFDAC number B4-3909, your pack's expiry date and batch number to get a Trust Score, compare the pack with the NAFDAC record (ingredient, strength, form, manufacturer), and buy only from licensed pharmacies.

How do I take Bioptan Eyedrops?

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…

What is Bioptan Eyedrops 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 ) (Summarised from the official U.S. FDA label for bimatoprost. Always follow your doctor or pharmacist.)

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