Description
NDC: 72266-140-01
Bimatoprost 0.03% Ophthalmic Solution, 5 mL — Fosun Pharma USA
| Active ingredients | Bimatoprost 0.3 mg/mL (0.03%) |
| Dosage form | Sterile ophthalmic solution |
| Route | Topical ophthalmic |
| Size | 5 mL |
| Manufacturer | Fosun Pharma USA |
| NDC | 72266-140-01 |
Indications and Usage
Reduction of elevated intraocular pressure in patients with open-angle glaucoma or ocular hypertension.
Dosage and Administration
Instill one drop in the affected eye(s) once daily in the evening. Do not exceed once-daily dosing, as more frequent administration may lessen the IOP-lowering effect; separate from other topical ophthalmic products by at least 5 minutes.
Warnings and Precautions
- May cause permanent increased brown iris pigmentation
- Eyelid skin darkening and eyelash changes (length, thickness, pigmentation), usually reversible
- Use caution in active intraocular inflammation or with risk factors for macular edema
- Remove contact lenses before instillation and reinsert 15 minutes later
Contraindications
Hypersensitivity to bimatoprost or any component of the formulation.
Adverse Reactions
The most common adverse reaction is conjunctival hyperemia; other reactions include eyelash growth, ocular pruritus, dryness, and irritation.
Storage and Handling
Store at 2°C to 25°C (36°F to 77°F).
How Supplied
Sterile ophthalmic solution in a low-density polyethylene dropper bottle with a controlled-drop tip and turquoise cap, packaged in a carton.
Professional use only. Clinical information summarized from FDA-approved prescribing information (Structured Product Labeling); refer to the full prescribing information via DailyMed for complete details.
If you have any questions related to DSCSA compliance, transaction history, regulatory data or quality assurance, please contact our team at compliance@dryeyerescue.com for more information.
