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Sandoz

Prednisolone Acetate Ophthalmic Suspension, USP 1%, 10 mL

SKU: RX-1082Medical Supplies

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NDC: 61314-637-10

Prednisolone Acetate Ophthalmic Suspension, USP 1%, 10 mL — Sandoz

Active ingredientPrednisolone acetate 1.0% (10 mg/mL)
PreservativeBenzalkonium chloride 0.01%
Dosage formOphthalmic suspension
RouteTopical ophthalmic
Size10 mL
ManufacturerManufactured by Alcon Laboratories, Inc., Fort Worth, TX for Sandoz Inc., Princeton, NJ

Indications and Usage

Indicated for steroid-responsive inflammatory conditions of the conjunctiva, cornea, and anterior segment, including allergic conjunctivitis, iritis, and cyclitis, as well as corneal injury from chemical, radiation, or thermal burns.

Dosage and Administration

SHAKE WELL BEFORE USING. Apply 2 drops in the affected eye(s) four times daily. Reevaluate if symptoms fail to improve after two days.

Warnings and Precautions

  • Prolonged use may cause glaucoma, optic nerve damage, or posterior subcapsular cataracts.
  • May suppress immune response and increase risk of secondary ocular infection, including fungal and viral infections.
  • May cause corneal or scleral thinning, with risk of perforation.
  • If used 10 days or longer, monitor intraocular pressure.

Contraindications

Most viral, fungal, and mycobacterial eye infections; known hypersensitivity to any ingredient or to other corticosteroids.

Storage

Store at 8°C to 24°C (46°F to 75°F) in an upright position.

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.

NDC
61314-637-10

Ships in 1–2 business days

Standard transit is 3–5 business days within the contiguous US. Tracking is included with every shipment.

30-day returns on unopened items

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