NDC 47335-321

Memantine Hydrochloride 5 mg tablet, film coated

On the label: Caraco Pharmaceutical Laboratories, Ltd..

Where it's made

Sun Pharmaceutical Industries Limited

Dadra, India · makes it and tests it

Problems found, fixed voluntarily Last FDA inspection Mar 29, 2019. 5 inspections on record.

Product details

Generic drug

Memantine: see every company that makes it

Form

tablet, film coated, oral

Strength

5 mg

Approval

ANDA ANDA090058

On the market since

Jul 11, 2015

Package NDCs

47335-321-08 47335-321-18 47335-321-86 47335-321-88

Official label

DailyMed (National Library of Medicine), updated Oct 5, 2023

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