NDC 65162-169

memantine hydrochloride 10 mg tablet, film coated

On the label: Amneal Pharmaceuticals.

India: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Amneal Pharmaceuticals Private LimitedAhmedabad, IndiaMakes it, tests it, packages it and labels it No problems foundJul 19, 2024 · 6 inspections

Product details

Generic drug
Memantine: every company that makes it
Form
tablet, film coated, oral
Strength
10 mg
Approval
ANDA ANDA090041
On the market since
Mar 24, 2022
Package NDCs
65162-169-06
Official label
DailyMed (National Library of Medicine), updated Dec 20, 2025

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