NDC 24208-504

Vyzulta 0.24 mg per 1 mL solution/ drops

On the label: Bausch & Lomb Incorporated.

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Bausch & Lomb IncorporatedTampa, FL, United StatesMakes it Serious problems, FDA actionMar 20, 2026 · 17 inspections, 3 with FDA action

Product details

Generic drug
Latanoprost Acid: every company that makes it
Form
solution/ drops, ophthalmic
Strength
0.24 mg per 1 mL
Approval
NDA NDA207795
On the market since
Nov 2, 2017
Package NDCs
24208-504-01 24208-504-02 24208-504-05 24208-504-06
Official label
DailyMed (National Library of Medicine), updated Feb 27, 2024

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