Travatan Indications, Dosage, Storage, Stability - Travoprost

Travatan Indications, Dosage, Storage, Stability - Travoprost INDICATIONS AND USES

TRAVATAN^® Ophthalmic Solution is indicated for the reduction of elevated intraocular pressure in patients with open-angle glaucoma or ocular hypertension who are intolerant of other intraocular pressure lowering medications or insufficiently responsive (failed to achieve target IOP determined after multiple measurements over time) to another intraocular pressure lowering medication.

The recommended dosage is one drop in the affected eye(s) once-daily in the evening. The dosage of TRAVATAN^® should not exceed once-daily since it has been shown that more frequent administration may decrease the intraocular pressure lowering effect.

Reduction of intraocular pressure starts approximately 2 hours after administration, and the maximum effect is reached after 12 hours.

TRAVATAN^® 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 (5) minutes apart.

TRAVATAN^® (travoprost ophthalmic solution) 0.004% is a sterile, isotonic, buffered, preserved, aqueous solution of travoprost (0.04 mg/mL) supplied in Alcon's oval DROP-TAINER® package system inside a sealed foil pouch.

TRAVATAN^® is supplied as a 2.5 mL solution in a 3.5 mL natural polypropylene dispenser bottle with a natural polypropylene dropper tip and a turquoise polypropylene overcap. Tamper evidence is provided with a shrink band around the closure and neck area of the package.

NDC 0065-0266-25, 2.5 mL fill
NDC 0065-0266-17, 2 units, 2.5 mL fill each
NDC 0065-0266-34, 5 mL fill

Storage
Store at 2^° - 25^°C (36^° - 77^°F).

Rx Only

U.S. Patent Nos. 5,631,287; 5,849,792; 5,889,052; 6,011,062, and 6,235,781.

*TIMOPTIC is a registered trademark of Merck & Co., Inc.

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