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HSA Approval

TOBREX STERILE OPHTHALMIC OINTMENT 0.3%

SIN04722P

TOBREX STERILE OPHTHALMIC OINTMENT 0.3%

TOBREX STERILE OPHTHALMIC OINTMENT 0.3%

June 13, 1990

NOVARTIS (SINGAPORE) PTE LTD

NOVARTIS (SINGAPORE) PTE LTD

Regulatory Information

HSA regulatory responsibility and product classification details

Regulatory Responsibility

RegistrantNOVARTIS (SINGAPORE) PTE LTD
Licence HolderNOVARTIS (SINGAPORE) PTE LTD

Product Classification

D
Drug Type
Therapeutic
F
Forensic Class
Prescription Only
HSA Singapore Classification

Formulation Information

OINTMENT

**4.2 Posology and method of administration** **Posology** As indicated by physician: In mild to moderate disease, apply a 1.5 centimetre ribbon into the affected eye(s) 2 or 3 times per day. In severe infections, instill a 1.5 centimetre ribbon into the eye(s) every 3 to 4 hours until improvement, following which treatment should be reduced prior to discontinuation. Tobrex ophthalmic ointment may be used in conjunction with Tobrex ophthalmic solution. Use in children The safety and efficacy of Tobrex® Ophthalmic Ointment in children younger than 1 year of age have not been established. Use in patients with hepatic or renal impairment The safety and efficacy of Tobrex® Ophthalmic Ointment in patients with hepatic or renal impairment have not been established. Use in elderly population No overall clinical differences in safety or efficacy have been observed between the elderly and other adult populations. **Method of administration** For ocular use. To avoid contamination, the tube tip should not touch any surface. The tube tip should also not come into contact with the eye as this may cause injury to the eye. Keep the tube tightly closed when not in use. Either nasolacrimal occlusion or gently closing the eyelid(s) after administration is recommended. This may reduce the systemic absorption of medicinal products administered via the ocular route and result in a decrease in systemic adverse reactions. If more than one topical ophthalmic product is being used, the products must be administered at least 5 minutes apart. Eye ointments should be administered last.

OPHTHALMIC

Medical Information

**4.1 Therapeutic indications** Tobrex® Ophthalmic Ointment contains tobramycin, a water-soluble aminoglycoside antibiotic active against a wide variety of gram- negative and gram-positive ophthalmic pathogens. Tobrex® Ophthalmic Ointment is a topical antibiotic indicated in the treatment of external infections of the eye and its adnexa, caused by susceptible bacteria. Appropriate monitoring of bacterial response to topical antibiotic therapy should accompany the use of Tobrex® Ophthalmic Ointment. Clinical studies have shown tobramycin to be safe and effective for use in children.

**4.3 Contraindications** Hypersensitivity to the active substance or to any of the excipients listed in section 6.1. – _please refer to the Product Insert/Patient Information Leaflet published on HSA for the full drug information._

S01AA12

tobramycin

Manufacturer Information

NOVARTIS (SINGAPORE) PTE LTD

ALCON-COUVREUR NV

Active Ingredients

TOBRAMYCIN

3 mg/g

Tobramycin

Documents

Package Inserts

Tobrex Ophthalmic Ointment PI.pdf

Approved: April 18, 2022

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