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HSA Product

ROCKLATAN OPHTHALMIC SOLUTION, 0.02% W/V / 0.005% W/V

Product approved by Health Sciences Authority (SG)

Basic Information

ROCKLATAN OPHTHALMIC SOLUTION, 0.02% W/V / 0.005% W/V

SOLUTION, STERILE

Regulatory Information

SIN16818P

July 4, 2023

Prescription Only

Therapeutic

OPHTHALMIC

August 10, 2023

May 30, 2025

XS01EE51

Company Information

SANTEN PHARMACEUTICAL ASIA PTE. LTD.

SANTEN PHARMACEUTICAL ASIA PTE. LTD.

Active Ingredients

Latanoprost

Strength: 0.005% w/v

Detailed Information

Contraindications

**4\. CONTRAINDICATIONS** Hypersensitivity to the active substance(s) or to any of the excipients.

Indication Information

**1\. INDICATIONS AND USAGE** ROCKLATAN (netarsudil and latanoprost ophthalmic solution) 0.02%/0.005% is a fixed dose combination of a Rho kinase inhibitor and a prostaglandin F2α analogue indicated for the reduction of elevated intraocular pressure (IOP) in patients with primary open-angle glaucoma or ocular hypertension for whom monotherapy with a prostaglandin F2α analogue or Rho kinase inhibitor provides insufficient IOP reduction.

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