NDC 55111-596

Memantine Hydrochloride 5 mg tablet, film coated

On the label: Dr.Reddy's Laboratories Ltd..

Where it's made

Dr. Reddy's Laboratories Limited

Medchal-Malkajgiri, India · makes it and tests it

Problems found, fixed voluntarily Last FDA inspection Oct 27, 2023. 8 inspections on record.

Product details

Generic drug

Memantine: see every company that makes it

Form

tablet, film coated, oral

Strength

5 mg

Approval

ANDA ANDA090048

On the market since

Jul 11, 2015

Package NDCs

55111-596-01 55111-596-05 55111-596-30 55111-596-60 55111-596-78 55111-596-79

Official label

DailyMed (National Library of Medicine), updated Feb 8, 2019

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