NDC 24208-463

Latanoprost 50 ug 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
50 ug per 1 mL
Approval
ANDA ANDA201006
On the market since
Mar 22, 2011
Package NDCs
24208-463-25
Official label
DailyMed (National Library of Medicine), updated Oct 23, 2025

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