April 23, 2017
Recommended Topic Related To:

Cosopt

"The US Food and Drug Administration (FDA) has approved ranibizumab injection (Lucentis, Genentech) in a prefilled syringe, the company has announced.

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Cosopt




Indications
Dosage
How Supplied

INDICATIONS

COSOPT® is indicated for the reduction of elevated intraocular pressure (IOP) in patients with open-angle glaucoma or ocular hypertension who are insufficiently responsive to beta-blockers (failed to achieve target IOP determined after multiple measurements over time). The IOP-lowering of COSOPT administered twice a day was slightly less than that seen with the concomitant administration of 0.5% timolol administered twice a day and 2% dorzolamide administered three times a day [see Clinical Studies].

DOSAGE AND ADMINISTRATION

The dose is one drop of COSOPT in the affected eye(s) two times daily.

If more than one topical ophthalmic drug is being used, the drugs should be administered at least five minutes apart [see DRUG INTERACTIONS].

HOW SUPPLIED

Dosage Forms And Strengths

Solution containing 20 mg/mL dorzolamide (22.26 mg of dorzolamide hydrochloride) and 5 mg/mL timolol (6.83 mg timolol maleate).

Storage And Handling

COSOPT Ophthalmic Solution is supplied in an OCUMETER® PLUS container, a white, translucent, HDPE plastic ophthalmic dispenser with a controlled drop tip and a white polystyrene cap with dark blue label as follows:

NDC 17478-605-10, 10 mL in an 18 mL capacity bottle.

Storage

Store COSOPT at 15° to 30°C (59° to 86°F). Protect from light.

Distributed by: Akorn, Inc., Lake Forest, IL 60045 Made in France. Revised: Jan 2015

This monograph has been modified to include the generic and brand name in many instances.

Last reviewed on RxList: 11/4/2016

Indications
Dosage
How Supplied

Cosopt - User Reviews

Cosopt User Reviews

Now you can gain knowledge and insight about a drug treatment with Patient Discussions.

Here is a collection of user reviews for the medication Cosopt sorted by most helpful. Patient Discussions FAQs

Report Problems to the Food and Drug Administration

 

You are encouraged to report negative side effects of prescription drugs to the FDA. Visit the FDA MedWatch website or call 1-800-FDA-1088.


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