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Prolensa

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Prolensa

INDICATIONS

PROLENSA™ (bromfenac ophthalmic solution) 0.07% is indicated for the treatment of postoperative inflammation and reduction of ocular pain in patients who have undergone cataract surgery.

DOSAGE AND ADMINISTRATION

Recommended Dosing

One drop of PROLENSA ophthalmic solution should be applied to the affected eye once daily beginning 1 day prior to cataract surgery, continued on the day of surgery, and through the first 14 days of the postoperative period.

Use with Other Topical Ophthalmic Medications

PROLENSA ophthalmic solution may be administered in conjunction with other topical ophthalmic medications such as alpha-agonists, beta-blockers, carbonic anhydrase inhibitors, cycloplegics, and mydriatics. Drops should be administered at least 5 minutes apart.

HOW SUPPLIED

Dosage Forms And Strengths

Topical ophthalmic solution: bromfenac 0.07%

Storage And Handling

PROLENSA (bromfenac ophthalmic solution) 0.07% is supplied in a white LDPE plastic squeeze bottle with a 15 mm LDPE white dropper-tip and 15 mm polypropylene gray cap as follows:

1.6 mL in a 7.5 mL container (NDC 24208-602-01)
3 mL in a 7.5 mL container (NDC 24208-602-03)

Storage

Store at 15° – 25°C (59° – 77°F).

Manufactured by: Bausch & Lomb Incorporated, Tampa, FL 33637. Revised: 4/2013

Last reviewed on RxList: 4/15/2013
This monograph has been modified to include the generic and brand name in many instances.

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