01 3Bausch & Lomb Incorporated
02 1GLAND PHARMA LIMITED
01 1OPD
02 1SOLUTION
03 2SOLUTION/DROPS;OPHTHALMIC
01 1Originator
02 1Prescription
03 2RX
01 1LATANOPROSTENE BUNOD
02 2VYZULTA
03 1Vyzulta
01 1Canada
02 1South Africa
03 2USA
Regulatory Info : RX
Registration Country : USA
Brand Name : VYZULTA
Dosage Form : SOLUTION/DROPS;OPHTHALMIC
Dosage Strength : 0.024%
Packaging :
Approval Date : 2017-11-02
Application Number : 207795
Regulatory Info : RX
Registration Country : USA
Regulatory Info : Prescription
Registration Country : Canada
Brand Name : VYZULTA
Dosage Form : SOLUTION
Dosage Strength : 0.024%/W/V
Packaging : 5ML
Approval Date :
Application Number : 2484218
Regulatory Info : Prescription
Registration Country : Canada
Regulatory Info : Originator
Registration Country : South Africa
Brand Name : Vyzulta
Dosage Form : OPD
Dosage Strength : 0,24mg/ml
Packaging : 5X1mg/ml
Approval Date :
Application Number :
Regulatory Info : Originator
Registration Country : South Africa
Regulatory Info : RX
Registration Country : USA
Brand Name : LATANOPROSTENE BUNOD
Dosage Form : SOLUTION/DROPS;OPHTHALMIC
Dosage Strength : 0.024%
Packaging :
Approval Date : 2025-04-29
Application Number : 217387
Regulatory Info : RX
Registration Country : USA
