NDC 53746-173

Memantine hydrochloride 5 mg tablet, film coated

On the label: Amneal Pharmaceuticals.

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Amneal Pharmaceuticals of New York, LLCBrookhaven, NY, United StatesMakes it, tests it, packages it and labels it No problems foundSep 25, 2026 · 14 inspections

Product details

Generic drug
Memantine: every company that makes it
Form
tablet, film coated, oral
Strength
5 mg
Approval
ANDA ANDA090041
On the market since
Apr 30, 2015
Package NDCs
53746-173-10 53746-173-30 53746-173-60
Official label
DailyMed (National Library of Medicine), updated Aug 17, 2023

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