NDC 33342-066

Memantine Hydrochloride 2 mg per 1 mL solution

On the label: Macleods Pharmaceuticals Limited.

Where it's made

Macleods Pharmaceuticals Limited

District Solan, India · makes it, tests it, packages it and labels it

Problems found, fixed voluntarily Last FDA inspection Oct 20, 2023. 6 inspections on record, 2 with serious problems.

Product details

Generic drug
Memantine: see every company that makes it
Form
solution, oral
Strength
2 mg per 1 mL
Approval
ANDA ANDA202790
On the market since
Oct 13, 2015
Package NDCs
33342-066-28
Official label
DailyMed (National Library of Medicine), updated Feb 9, 2023

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