FDA label
What is Lumigan used for?
Lumigan contains bimatoprost. The FDA-approved uses below are quoted from the Indications and Usage section of its DailyMed label.
Source: DailyMed SPL label file dated 2026-10-23. Publisher page
The FDA label says: “LUMIGAN ® (bimatoprost ophthalmic solution) 0.01% is indicated for the reduction of elevated intraocular pressure in patients with open angle glaucoma or ocular hypertension.”
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Lumigan, solution/ drops
Indications and Usage, quoted from the label by Allergan, Inc. (NDA022184). Cross-references to other label sections are left out.
LUMIGAN ® (bimatoprost ophthalmic solution) 0.01% is indicated for the reduction of elevated intraocular pressure in patients with open angle glaucoma or ocular hypertension.
Source: DailyMed label, set id a5e67c75-db88-4372-bb07-c8dd15c97631, version 19, effective June 22, 2024. NDC 0023-3205, one of 1 listing for this product.
Questions
What is Lumigan used for?
The FDA label says: “LUMIGAN ® (bimatoprost ophthalmic solution) 0.01% is indicated for the reduction of elevated intraocular pressure in patients with open angle glaucoma or ocular hypertension.”
What drug class is Lumigan?
FDA lists bimatoprost in the Prostaglandin Analog established pharmacologic class.
Does this page cover off-label uses or dosing?
No. This page shows only the Indications and Usage section of the FDA label. Ask a pharmacist or prescriber about dosing.
More on Lumigan
- Is Lumigan a controlled substance?Federal schedule
- Generic for LumiganFDA Orange Book
- What is Bimatoprost used for?FDA label uses
- Is Bimatoprost a controlled substance?Federal schedule
- Generic for ZolymbusFDA Orange Book
- Generic for DurystaFDA Orange Book
- Generic for LatisseFDA Orange Book
- Prostaglandin Analogs listFDA drug class
- Lumigan Medicare Part D coverageBy plan and state
- NDC 0023-3205Lumigan NDC record