NDC 67046-458

Memantine Hydrochloride 10 mg tablet, film coated

On the label: Coupler Enterprises Inc.. It's a repackaged product: Coupler Enterprises Inc. rebottles it from Caraco Pharmaceutical Laboratories, Ltd.'s NDC 47335-322.

Where the pills inside were 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.

Repackaging site

• Coupler Enterprises, · repackages it

Product details

Generic drug

Memantine: see every company that makes it

Form

tablet, film coated

Strength

10 mg

Approval

ANDA ANDA090058

On the market since

Sep 28, 2017

Package NDCs

67046-458-07 67046-458-14 67046-458-15 67046-458-20 67046-458-21 67046-458-28 67046-458-30 67046-458-60

Official label

DailyMed (National Library of Medicine), updated Sep 28, 2017

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