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HSA Approval

Taflotan Ophthalmic Solution 0.0015%

SIN13872P

Taflotan Ophthalmic Solution 0.0015%

Taflotan Ophthalmic Solution 0.0015%

October 7, 2010

SANTEN PHARMACEUTICAL ASIA PTE. LTD.

SANTEN PHARMACEUTICAL ASIA PTE. LTD.

Regulatory Information

HSA regulatory responsibility and product classification details

Regulatory Responsibility

RegistrantSANTEN PHARMACEUTICAL ASIA PTE. LTD.
Licence HolderSANTEN PHARMACEUTICAL ASIA PTE. LTD.

Product Classification

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

Formulation Information

SOLUTION, STERILE

**Dosage and Administration** Instill 1 drop in the affected eye(s) once daily. **<Precautions>** Do not use more than once daily because more frequent administration may lessen the IOP-lowering effect.

OPHTHALMIC

Medical Information

**Indications** Reduction of intraocular pressure in patients with primary open-angle glaucoma or ocular hypertension.

**Contraindications (This product is contraindicated in the following patients.)** Patients with a history of hypersensitivity to any of the ingredients of this product. Patients with combination with products containing omidenepag isopropyl.

S01EE05

tafluprost

Manufacturer Information

SANTEN PHARMACEUTICAL ASIA PTE. LTD.

Santen Pharmaceutical Co., Ltd. Shiga Plant

Active Ingredients

Tafluprost

0.015mg/ml

Tafluprost

Documents

Package Inserts

PI_Taflotan_Singapore.pdf

Approved: October 7, 2021

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Taflotan Ophthalmic Solution 0.0015% - HSA Approval | MedPath