NDC 65862-652

Memantine Hydrochloride 5 mg tablet, film coated

On the label: Aurobindo Pharma Limited.

Where it's made

Aurobindo Pharma Limited

Mahabubnagar, India · makes it and tests it

Problems found, fixed voluntarily Last FDA inspection May 10, 2022. 7 inspections on record, 1 with serious problems.

Product details

Generic drug

Memantine: see every company that makes it

Form

tablet, film coated, oral

Strength

5 mg

Approval

ANDA ANDA203175

On the market since

Oct 13, 2015

Package NDCs

65862-652-03 65862-652-10 65862-652-60 65862-652-78 65862-652-99

Official label

DailyMed (National Library of Medicine), updated Nov 8, 2022

Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?