NDC 65862-872

Latanoprost 50 ug per 1 mL solution/ drops

On the label: Aurobindo Pharma Limited.

India: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Eugia Pharma Specialities LimitedSangareddy, IndiaMakes it, tests it and packages it Serious problems, FDA actionFeb 6, 2026 · 7 inspections, 2 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 ANDA206519
On the market since
Sep 3, 2019
Package NDCs
65862-872-25
Official label
DailyMed (National Library of Medicine), updated Sep 27, 2024

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