COSOPT PF Dailymed

7 Drug Interactions

• Potential additive effect of oral carbonic anhydrase inhibitor with COSOPT PF. (7.1)
• Potential acid-base and electrolyte disturbances. (7.2)
• Concomitant use with systemic beta-blockers may potentiate systemic beta-blockade. (7.3)
• Oral or intravenous calcium antagonists may cause atrioventricular conduction disturbances, left ventricular failure, and hypotension. (7.4)
• Catecholamine-depleting drugs may have additive effects and produce hypotension and/or marked bradycardia. (7.5)
• Digitalis and calcium antagonists may have additive effects in prolonging atrioventricular conduction time. (7.6)
• CYP2D6 inhibitors may potentiate systemic beta-blockade. (7.7)

7.1 Oral Carbonic Anhydrase Inhibitors

There is a potential for an additive effect on the known systemic effects of carbonic anhydrase inhibition in patients receiving an oral carbonic anhydrase inhibitor and COSOPT PF. The concomitant administration of COSOPT PF and oral carbonic anhydrase inhibitors is not recommended.

7.2 High-Dose Salicylate Therapy

Although acid-base and electrolyte disturbances were not reported in the clinical trials with dorzolamide hydrochloride ophthalmic solution, these disturbances have been reported with oral carbonic anhydrase inhibitors and have, in some instances, resulted in drug interactions (e.g., toxicity associated with high-dose salicylate therapy). Therefore, the potential for such drug interactions should be considered in patients receiving COSOPT PF.

7.3 Beta-Adrenergic Blocking Agents

Patients who are receiving a beta-adrenergic blocking agent orally and COSOPT PF should be observed for potential additive effects of beta-blockade, both systemic and on intraocular pressure. The concomitant use of two topical beta-adrenergic blocking agents is not recommended.

7.4 Calcium Antagonists

Caution should be used in the coadministration of beta-adrenergic blocking agents, such as COSOPT PF, and oral or intravenous calcium antagonists because of possible atrioventricular conduction disturbances, left ventricular failure, and hypotension. In patients with impaired cardiac function, coadministration should be avoided.

7.5 Catecholamine-Depleting Drugs

Close observation of the patient is recommended when a beta-blocker is administered to patients receiving catecholamine-depleting drugs such as reserpine, because of possible additive effects and the production of hypotension and/or marked bradycardia, which may result in vertigo, syncope, or postural hypotension.

7.6 Digitalis and Calcium Antagonists

The concomitant use of beta-adrenergic blocking agents with digitalis and calcium antagonists may have additive effects in prolonging atrioventricular conduction time.

7.7 CYP2D6 Inhibitors

Potentiated systemic beta-blockade (e.g., decreased heart rate, depression) has been reported during combined treatment with CYP2D6 inhibitors (e.g., quinidine, SSRIs) and timolol.

7.8 Clonidine

Oral beta-adrenergic blocking agents may exacerbate the rebound hypertension which can follow the withdrawal of clonidine. There have been no reports of exacerbation of rebound hypertension with ophthalmic timolol maleate.

8 Use In Specific Populations

8.1 Pregnancy

TERATOGENIC EFFECTS SECTION

Teratogenic Effects. Pregnancy Category C. Developmental toxicity studies with dorzolamide hydrochloride in rabbits at oral doses of ≥2.5 mg/kg/day (31 times the recommended human ophthalmic dose) revealed malformations of the vertebral bodies. These malformations occurred at doses that caused metabolic acidosis with decreased body weight gain in dams and decreased fetal weights. No treatment-related malformations were seen at 1 mg/kg/day (13 times the recommended human ophthalmic dose).

Teratogenicity studies with timolol in mice, rats, and rabbits at oral doses up to 50 mg/kg/day (7,000 times the systemic exposure following the maximum recommended human ophthalmic dose) demonstrated no evidence of fetal malformations. Although delayed fetal ossification was observed at this dose in rats, there were no adverse effects on postnatal development of offspring. Doses of 1000 mg/kg/day (142,000 times the systemic exposure following the maximum recommended human ophthalmic dose) were maternotoxic in mice and resulted in an increased number of fetal resorptions. Increased fetal resorptions were also seen in rabbits at doses of 14,000 times the systemic exposure following the maximum recommended human ophthalmic dose, in this case without apparent maternotoxicity.

There are no adequate and well-controlled studies in pregnant women. COSOPT PF should be used during pregnancy only if the potential benefit justifies the potential risk to the fetus.

8.3 Nursing Mothers

It is not known whether dorzolamide is excreted in human milk. Timolol maleate has been detected in human milk following oral and ophthalmic drug administration. Because of the potential for serious adverse reactions from COSOPT PF in nursing infants, a decision should be made whether to discontinue nursing or to discontinue the drug, taking into account the importance of the drug to the mother.

8.4 Pediatric Use

The safety and effectiveness of dorzolamide hydrochloride ophthalmic solution and timolol maleate ophthalmic solution have been established when administered individually in pediatric patients aged 2 years and older. Use of these drug products in these children is supported by evidence from adequate and well-controlled studies in children and adults. Safety and efficacy in pediatric patients below the age of 2 years have not been established.

8.5 Geriatric Use

No overall differences in safety or effectiveness have been observed between elderly and younger patients.

10 Overdosage

Symptoms consistent with systemic administration of beta-blockers or carbonic anhydrase inhibitors may occur, including electrolyte imbalance, development of an acidotic state, dizziness, headache, shortness of breath, bradycardia, bronchospasm, cardiac arrest and possible central nervous system effects. Serum electrolyte levels (particularly potassium) and blood pH levels should be monitored. [See Adverse Reactions (6).]

A study of patients with renal failure showed that timolol did not dialyze readily.

11 Description

COSOPT PF (dorzolamide hydrochloride-timolol maleate ophthalmic solution) is the combination of a topical carbonic anhydrase inhibitor and a topical beta-adrenergic receptor blocking agent.

Dorzolamide hydrochloride is described chemically as: (4S-trans)-4-(ethylamino)-5,6-dihydro-6-methyl-4H-thieno[2,3-b]thiopyran-2-sulfonamide 7,7-dioxide monohydrochloride. Dorzolamide hydrochloride is optically active. The specific rotation is:

•   [α]        25°C        (C=1, water) = ~ -17°.
•                405 nm

Its empirical formula is C₁₀H₁₆N₂O₄S₃•HCl and its structural formula is:

Dorzolamide hydrochloride has a molecular weight of 360.91. It is a white to off-white, crystalline powder, which is soluble in water and slightly soluble in methanol and ethanol.

Timolol maleate is described chemically as: (-)-1-(tert-butylamino)-3-[(4-morpholino-1,2,5-thiadiazol-3-yl)oxy]-2-propanol maleate (1:1) (salt). Timolol maleate possesses an asymmetric carbon atom in its structure and is provided as the levo-isomer. The optical rotation of timolol maleate is:

•   [α]        25°C       in 1N HCl (C = 5) = -12.2° (-11.7° to -12.5°).
•                405 nm

Its molecular formula is C₁₃H₂₄N₄O₃S•C₄H₄O₄ and its structural formula is:

Timolol maleate has a molecular weight of 432.50. It is a white, odorless, crystalline powder which is soluble in water, methanol, and alcohol. Timolol maleate is stable at room temperature.

COSOPT PF is supplied as a sterile, clear, colorless to nearly colorless, isotonic, buffered, slightly viscous, aqueous solution. The pH of the solution is approximately 5.65, and the osmolarity is 242-323 mOsM. Each mL of COSOPT PF contains 20 mg dorzolamide (22.26 mg of dorzolamide hydrochloride) and 5 mg timolol (6.83 mg timolol maleate). Inactive ingredients are sodium citrate, hydroxyethyl cellulose, sodium hydroxide, mannitol, and water for injection.

COSOPT PF does not contain a preservative.

12 Clinical Pharmacology

12.1 Mechanism of Action

COSOPT PF is comprised of two components: dorzolamide hydrochloride and timolol maleate. Each of these two components decreases elevated intraocular pressure, whether or not associated with glaucoma, by reducing aqueous humor secretion. Elevated intraocular pressure is a major risk factor in the pathogenesis of optic nerve damage and glaucomatous visual field loss. The higher the level of intraocular pressure, the greater the likelihood of glaucomatous field loss and optic nerve damage.

Dorzolamide hydrochloride is an inhibitor of human carbonic anhydrase II. Inhibition of carbonic anhydrase in the ciliary processes of the eye decreases aqueous humor secretion, presumably by slowing the formation of bicarbonate ions with subsequent reduction in sodium and fluid transport. Timolol maleate is a beta₁ and beta₂ (non-selective) adrenergic receptor blocking agent that does not have significant intrinsic sympathomimetic, direct myocardial depressant, or local anesthetic (membrane-stabilizing) activity. The combined effect of these two agents administered as COSOPT PF administered twice daily results in additional intraocular pressure reduction compared to either component administered alone, but the reduction is not as much as when dorzolamide administered three times daily and timolol twice daily are administered concomitantly. [See Clinical Studies (14).]

12.3 Pharmacokinetics

Dorzolamide Hydrochloride

When topically applied, dorzolamide reaches the systemic circulation. To assess the potential for systemic carbonic anhydrase inhibition following topical administration, drug and metabolite concentrations in RBCs and plasma and carbonic anhydrase inhibition in RBCs were measured. Dorzolamide accumulates in RBCs during chronic dosing as a result of binding to CA-II. The parent drug forms a single N-desethyl metabolite, which inhibits CA-II less potently than the parent drug but also inhibits CA-I. The metabolite also accumulates in RBCs where it binds primarily to CA-I. Plasma concentrations of dorzolamide and metabolite are generally below the assay limit of quantitation (15nM). Dorzolamide binds moderately to plasma proteins (approximately 33%).

Dorzolamide is primarily excreted unchanged in the urine; the metabolite also is excreted in urine. After dosing is stopped, dorzolamide washes out of RBCs nonlinearly, resulting in a rapid decline of drug concentration initially, followed by a slower elimination phase with a half-life of about four months.

To simulate the systemic exposure after long-term topical ocular administration, dorzolamide was given orally to eight healthy subjects for up to 20 weeks. The oral dose of 2 mg twice daily closely approximates the amount of drug delivered by topical ocular administration of dorzolamide 2% three times daily. Steady state was reached within 8 weeks. The inhibition of CA-II and total carbonic anhydrase activities was below the degree of inhibition anticipated to be necessary for a pharmacological effect on renal function and respiration in healthy individuals.

Timolol Maleate

In a study of plasma drug concentrations in six subjects, the systemic exposure to timolol was determined following twice daily topical administration of timolol maleate ophthalmic solution 0.5%. The mean peak plasma concentration following morning dosing was 0.46 ng/mL.

13 Nonclinical Toxicology

13.1 Carcinogenesis, Mutagenesis, Impairment of Fertility

In a two-year study of dorzolamide hydrochloride administered orally to male and female Sprague-Dawley rats, urinary bladder papillomas were seen in male rats in the highest dosage group of 20 mg/kg/day (250 times the recommended human ophthalmic dose). Papillomas were not seen in rats given oral doses equivalent to approximately 12 times the recommended human ophthalmic dose. No treatment-related tumors were seen in a 21-month study in female and male mice given oral doses up to 75 mg/kg/day (~900 times the recommended human ophthalmic dose).

The increased incidence of urinary bladder papillomas seen in the high-dose male rats is a class-effect of carbonic anhydrase inhibitors in rats. Rats are particularly prone to developing papillomas in response to foreign bodies, compounds causing crystalluria, and diverse sodium salts.

No changes in bladder urothelium were seen in dogs given oral dorzolamide hydrochloride for one year at 2 mg/kg/day (25 times the recommended human ophthalmic dose) or monkeys dosed topically to the eye at 0.4 mg/kg/day (~5 times the recommended human ophthalmic dose) for one year.

In a two-year study of timolol maleate administered orally to rats, there was a statistically significant increase in the incidence of adrenal pheochromocytomas in male rats administered 300 mg/kg/day (approximately 42,000 times the systemic exposure following the maximum recommended human ophthalmic dose). Similar differences were not observed in rats administered oral doses equivalent to approximately 14,000 times the maximum recommended human ophthalmic dose.

In a lifetime oral study of timolol maleate in mice, there were statistically significant increases in the incidence of benign and malignant pulmonary tumors, benign uterine polyps and mammary adenocarcinomas in female mice at 500 mg/kg/day, (approximately 71,000 times the systemic exposure following the maximum recommended human ophthalmic dose), but not at 5 or 50 mg/kg/day (approximately 700 or 7,000, respectively, times the systemic exposure following the maximum recommended human ophthalmic dose). In a subsequent study in female mice, in which post-mortem examinations were limited to the uterus and the lungs, a statistically significant increase in the incidence of pulmonary tumors was again observed at 500 mg/kg/day.

The increased occurrence of mammary adenocarcinomas was associated with elevations in serum prolactin which occurred in female mice administered oral timolol at 500 mg/kg/day, but not at doses of 5 or 50 mg/kg/day. An increased incidence of mammary adenocarcinomas in rodents has been associated with administration of several other therapeutic agents that elevate serum prolactin, but no correlation between serum prolactin levels and mammary tumors has been established in humans. Furthermore, in adult human female subjects who received oral dosages of up to 60 mg of timolol maleate (the maximum recommended human oral dosage), there were no clinically meaningful changes in serum prolactin.

The following tests for mutagenic potential were negative for dorzolamide: (1) in vivo (mouse) cytogenetic assay; (2) in vitro chromosomal aberration assay; (3) alkaline elution assay; (4) V-79 assay; and (5) Ames test.

Timolol maleate was devoid of mutagenic potential when tested in vivo (mouse) in the micronucleus test and cytogenetic assay (doses up to 800 mg/kg) and in vitro in a neoplastic cell transformation assay (up to 100 μg/mL). In Ames tests the highest concentrations of timolol employed, 5,000 or 10,000 μg/plate, were associated with statistically significant elevations of revertants observed with tester strain TA100 (in seven replicate assays), but not in the remaining three strains. In the assays with tester strain TA100, no consistent dose response relationship was observed, and the ratio of test to control revertants did not reach 2. A ratio of 2 is usually considered the criterion for a positive Ames test.

Reproduction and fertility studies in rats with either timolol maleate or dorzolamide hydrochloride demonstrated no adverse effect on male or female fertility at doses up to approximately 100 times the systemic exposure following the maximum recommended human ophthalmic dose.

14 Clinical Studies

14.1 COSOPT Efficacy

Clinical studies of 3 to 15 months duration were conducted to compare the IOP-lowering effect over the course of the day of COSOPT twice daily (dosed morning and bedtime) to individually- and concomitantly-administered 0.5% timolol twice daily and 2.0% dorzolamide twice and three times daily. The IOP-lowering effect of COSOPT twice daily was greater (1-3 mmHg) than that of monotherapy with either 2.0% dorzolamide three times daily or 0.5% timolol twice daily. The IOP-lowering effect of COSOPT twice daily was approximately 1 mmHg less than that of concomitant therapy with 2.0% dorzolamide three times daily and 0.5% timolol twice daily.

Open-label extensions of two studies were conducted for up to 12 months. During this period, the IOP-lowering effect of COSOPT twice daily was consistent during the 12 month follow-up period.

14.2 COSOPT PF Equivalence Study

In an active-treatment controlled, parallel, double-masked study in 261 patients with elevated intraocular pressure ≥22 mmHg in one or both eyes, COSOPT PF had an IOP-lowering effect equivalent to that of COSOPT.

16 How Supplied/storage And Handling

COSOPT PF is supplied in a foil pouch containing 15 low density polyethylene 0.2 mL single-use containers.

NDC 17478-604-30, package of 60 single-use vials.

NDC 17478-604-90, package of 180 single-use vials.

Store COSOPT PF at 20° to 25°C (68° to 77°F). Do not freeze.

Store in the original pouch. After the pouch is opened, store the remaining single-use containers in the foil pouch to protect from light. Write down the date you open the foil pouch in the space provided on the pouch. Discard any unused containers 15 days after first opening the pouch.

17 Patient Counseling Information

See FDA-Approved Patient Labeling (Patient Information).

17.1 Potential for Exacerbation of Asthma and COPD

COSOPT PF may cause severe worsening of asthma and COPD symptoms including death due to bronchospasm. Patients with bronchial asthma, a history of bronchial asthma, severe chronic obstructive pulmonary disease should be advised not to take this product. [See Contraindications (4.1).]

17.2 Potential of Cardiovascular Effects

COSOPT PF may cause worsening of cardiac symptoms. Patients with sinus bradycardia, second or third degree atrioventricular block, or cardiac failure should be advised not to take this product. [See Contraindications (4.2).]

17.3 Sulfonamide Reactions

COSOPT PF contains dorzolamide (which is a sulfonamide) and, although administered topically, is absorbed systemically. Therefore the same types of adverse reactions that are attributable to sulfonamides may occur with topical administration, including severe skin reactions. Patients should be advised that if serious or unusual reactions or signs of hypersensitivity occur, they should discontinue the use of the product and seek their physician's advice. [See Warnings and Precautions (5.3).]

17.4 Handling the Single-Use Container

COSOPT PF is a sterile solution that does not contain a preservative. The solution from one individual unit is to be used immediately after opening for administration to one or both eyes. Since sterility cannot be maintained after the individual unit is opened, the remaining contents should be discarded immediately after administration.

17.5 Intercurrent Ocular Conditions

Patients also should be advised that if they have ocular surgery or develop an intercurrent ocular condition (e.g., trauma or infection), they should immediately seek their physician's advice concerning the continued use of this product.

17.6 Concomitant Topical Ocular Therapy

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

AKORN Distributed by: Akorn, Inc.Lake Forest, IL 60045

The COSOPT trademark is owned by Merck Sharp & Dohme Corp. and is used under license.

PF00N      Revision 06/2017

AK60301

Spl Patient Package Insert Section

Patient Information

COSOPT ^® PF (CO-sopt PEA EHF)

(dorzolamide hydrochloride-timolol maleate ophthalmic solution) 2%/0.5%

Read this information before you start using COSOPT PF and each time you get a refill. There may be new information. This information does not take the place of talking to your doctor about your medical condition or your treatment.

What is COSOPT PF?

COSOPT PF is a prescription sterile eye drop solution that contains 2 medicines, dorzolamide hydrochloride (a sulfonamide carbonic anhydrase inhibitor) and timolol maleate (a beta-adrenergic blocker). COSOPT PF is used to lower the pressure in the eye (intraocular pressure) in people with open-angle glaucoma or ocular hypertension, when their eye pressure is too high and beta-adrenergic blocker medicines alone have not adequately lowered the pressure.

It is not known if COSOPT PF is safe and effective in children under 2 years of age.

Who should not use COSOPT PF?

Do not use COSOPT PF if you:

• have or have had asthma
• have or have had severe lung problems (chronic obstructive pulmonary disease)
• have heart problems, including slow or irregular heartbeat or heart failure
• are allergic to dorzolamide hydrochloride, timolol maleate, or any of the ingredients in COSOPT PF. See the end of this leaflet for a complete ul of ingredients in COSOPT PF.

Talk to your healthcare provider before taking this medicine if you have any of these conditions.

What should I tell my doctor before using COSOPT PF?

Before you use COSOPT PF, tell your doctor if you:

• have problems with muscle weakness (myasthenia gravis)
• have diabetes or problems with low blood sugar (hypoglycemia)
• have thyroid, kidney, or liver problems
• are planning to have surgery
• are allergic to sulfa drugs
• have or have had eye problems, including any surgery on your eye or eyes, or are using any other eye medicines
• have any other medical problems
• are pregnant or plan to become pregnant. It is not known if COSOPT PF will harm your unborn baby. If you become pregnant while using COSOPT PF talk to your doctor right away.
• are breastfeeding or plan to breastfeed. It is not known whether dorzolamide passes into your breast milk however, timolol has been detected in breast milk. Talk to your doctor about the best way to feed your baby if you use COSOPT PF.

Tell your doctor about all the medicines you take, including prescription and non-prescription medicines, vitamins, and herbal supplements.

COSOPT PF and other medicines may affect each other causing side effects. COSOPT PF may affect the way other medicines work, and other medicines may affect how COSOPT PF works.

Know the medicines you take. Keep a ul of them to show your doctor and pharmacist when you get a new medicine.

How should I use COSOPT PF?

Read the Instructions for Use at the end of this Patient Information leaflet for additional instructions about the right way to use COSOPT PF.

• Use COSOPT PF exactly as your doctor tells you.
• Use 1 drop of COSOPT PF in your eye (or eyes) in the morning and 1 drop in the evening.
• If you use other medicines in your eye, wait at least 5 minutes between using COSOPT PF and your other eye medicines.
• Use your COSOPT PF right away after opening. Each COSOPT PF single-use container is sterile and is to be used 1 time then thrown away.
• Do not save any COSOPT PF that may be left over after you use a single-use container. Using COSOPT PF that is not sterile may cause other eye problems.

What are the possible side effects of COSOPT PF?

COSOPT PF may cause serious side effects including:

• severe breathing problems. These breathing problems can happen in people who have asthma, chronic obstructive pulmonary disease, or heart failure and can cause death. Tell your doctor right away if you have breathing problems while taking COSOPT PF.
• heart failure. This can happen in people who already have heart failure and in people who have never had heart failure before.Tell your doctor right away if you get any of these symptoms of heart failure while taking COSOPT PF:
  • shortness of breath
  • irregular heartbeat (palpitations)
  • swelling of your ankles or feet
  • sudden weight gain
• severe allergic reactions. These allergic reactions can happen the first time you use COSOPT PF or after you have been using COSOPT PF for a while and may cause death. Stop taking COSOPT PF and call your doctor right away or get emergency help if you get any of these symptoms of an allergic reaction:
  • swelling of your face, lips, mouth, or tongue
  • trouble breathing
  • wheezing
  • severe itching
  • skin rash, redness, or swelling
  • dizziness or fainting
  • fast heartbeat or pounding in your chest (tachycardia)
  • sweating
• worsening muscle weakness. COSOPT PF can cause muscle weakness to get worse in people who already have problems with muscle weakness (myasthenia gravis).
• kidney problems. Your doctor may do tests to check your kidney function while you use COSOPT PF.
• swelling of your eye (cornea)

The most common side effects of COSOPT PF include:

• a bitter, sour, or unusual taste in your mouth after using COSOPT PF
• burning, stinging, redness, or itching of the eye
• blurred vision
• painful, red, watery eyes with increased sensitivity (superficial punctate keratitis)

Tell your doctor if you have any new eye problems while using COSOPT PF including:

• an eye injury
• an eye infection
• a sudden loss of vision
• eye surgery
• swelling and redness of and around your eye (conjunctivitis)
• problems with your eyelids

Tell your doctor if you have any other side effects that bother you.

These are not all the possible side effects of COSOPT PF. For more information, ask your doctor or pharmacist.

Call your doctor about medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.

What should I do in case of an overdose?

If you swallow the contents of the container, contact your doctor immediately. Among other effects, you may feel light-headed, have difficulty breathing, or feel your heart rate has slowed.

How should I store COSOPT PF?

• Store COSOPT PF at room temperature between 68°F to 77°F (20°C to 25°C). Do not freeze.
• Keep the COSOPT PF single-use containers in their original foil pouch to protect from light.
• Write down the date you open the foil pouch in the space provided on the pouch.
• Throw away all unused COSOPT PF single-use containers 15 days after first opening the pouch.

Keep COSOPT PF and all medicines out of the reach of children.

General information about the safe and effective use of COSOPT PF.

Medicines are sometimes prescribed for purposes other than those uled in a Patient Information leaflet. Do not use COSOPT PF for a condition for which it was not prescribed. Do not give COSOPT PF to other people, even if they have the same symptoms you have. It may harm them. This Patient Information leaflet summarizes the most important information about COSOPT PF. If you would like more information, talk with your doctor. You can ask your pharmacist or doctor for information about COSOPT PF that is written for health professionals.

What are the ingredients in COSOPT PF?

Active ingredients: dorzolamide hydrochloride and timolol maleate

Inactive ingredients: sodium citrate, hydroxyethyl cellulose, sodium hydroxide, mannitol, and water for injection.

Instructions for Use

Read these instructions before using your COSOPT PF and each time you get a refill. There may be new information. This leaflet does not take the place of talking with your doctor about your medical condition or your treatment.

Important:

• COSOPT PF is for the eye only. Do not swallow COSOPT PF.
• COSOPT PF single-use containers are packaged in a foil pouch.
• Write down the date you open the foil pouch in the space provided on the pouch.

Every time you use COSOPT PF:

Step 1. Wash your hands.

Step 2. Take the strip of single-use containers from the pouch.

Step 3. Pull off 1 single-use container from the strip.

Step 4. Put the remaining strip of single-use containers back in the pouch and fold the edge to close the pouch.

Step 5. Hold the single-use container upright. Make sure that the solution is in the bottom part of the single-use container (See Figure A).

Step 6. Open the single-use container by twisting off the tab (See Figure B).

Step 7. Tilt your head backwards. If you are unable to tilt your head, lie down.

Step 8. Place the tip of the single-use container close to your eye. Be careful not to touch your eye with the tip of the single-use container

(See Figure C).

Step 9. Pull the lower eyelid downwards and look up.

Step 10. Gently squeeze the container and let 1 drop of COSOPT PF fall into the space between your lower eyelid and your eye. If a drop misses your eye, try again (See Figure D).

Step 11. Blot any excess solution from the skin around the eye with a tissue.

• If your doctor has told you to use drops in both eyes, repeat steps 7 to 11 for your other eye.
• There is enough COSOPT PF in 1 single-use container for 1 or both of your eyes.
• Throw away the opened single-use container with any remaining COSOPT PF right away.

This Patient Information and Instructions for Use have been approved by the U.S. Food and Drug Administration.

AKORN Distributed by: Akorn, Inc.Lake Forest, IL 60045

The COSOPT trademark is owned by Merck Sharp & Dohme Corp. and is used under license.

PF00N Rev. 06/17

AK60301

Package Label.principal Display Panel

Principal Display Panel Text for Container Label:

COSOPT^® PF 2% / 0.5%

(dorzolamide HCl – timolol

maleate ophthalmic solution)

Rx only

Package Label.principal Display Panel

Principal Display Panel Text for pouch Label:

NDC 17478-604-01

COSOPT^® PF

(dorzolamide HCl – timolol maleate

ophthalmic solution) 2% / 0.5%

For Topical Application in the Eye

Sterile Preservative-Free

Package Label.principal Display Panel

Principal Display Panel Text for Carton Label:

NDC 17478-604-30

COSOPT^® PF

(dorzolamide HCl – timolol maleate

ophthalmic solution) 2% / 0.5%

For Topical Application in the Eye

Sterile Preservative-Free