NDC 68382-548

Memantine hydrochloride 21 mg capsule, extended release

On the label: Zydus Pharmaceuticals (USA) Inc..

Where it's made

Zydus Lifesciences Limited

Ahmedabad, India · makes it and tests it

Problems found, fixed voluntarily Last FDA inspection Aug 5, 2022. 10 inspections on record, 3 with serious problems.

Product details

Generic drug

Memantine: see every company that makes it

Form

capsule, extended release, oral

Strength

21 mg

Approval

ANDA ANDA203293

On the market since

Apr 8, 2018

Package NDCs

68382-548-06 68382-548-16 68382-548-30 68382-548-77

Official label

DailyMed (National Library of Medicine), updated Oct 30, 2023

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