NDC 72189-467

Lamotrigine ER 200 mg tablet, extended release

On the label: Direct Rx. It's repackaged: Direct Rx rebottles it from Zydus Pharmaceuticals (USA) Inc.'s NDC 68382-982.

India: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Zydus Lifesciences LimitedAhmedabad, IndiaMakes it and tests it Problems found, fixed voluntarilyMar 24, 2023 · 5 inspections

Repackaging site

Product details

Generic drug
Lamotrigine: every company that makes it
Form
tablet, extended release, oral
Strength
200 mg
Approval
ANDA ANDA207763
On the market since
May 3, 2023
Package NDCs
72189-467-30
Official label
DailyMed (National Library of Medicine), updated Jan 22, 2025

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