Drugplain

Lamotrigine Extended-Release 300 mg/1

lamotrigine · TABLET, FILM COATED, EXTENDED RELEASE · Par Health USA, LLC

No Recall HistoryCurrently in Shortage
Plain English

Lamotrigine Extended-Release is a prescription anti-epileptic medication used to treat seizure disorders and certain mood conditions. This extended-release tablet is taken by mouth and allows for once-daily dosing compared to immediate-release forms.

Key Facts

Brand Name
Lamotrigine Extended-Release
Generic Name
lamotrigine
NDC Code (Product)
10370-256
Manufacturer
Par Health USA, LLC
Strength
300 mg/1
Dosage Form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Marketing Status
Application #
ANDA201374
Drug Class
Anti-epileptic Agent [EPC]; Mood Stabilizer [EPC]
Marketing Start
01/02/2026

Recall History

No Recall History

Frequently Asked Questions

What is Lamotrigine Extended-Release used for?

Lamotrigine Extended-Release is a prescription anti-epileptic medication used to treat seizure disorders and certain mood conditions. This extended-release tablet is taken by mouth and allows for once-daily dosing compared to immediate-release forms.

Is Lamotrigine Extended-Release a controlled substance?

Lamotrigine Extended-Release is not classified as a controlled substance by the DEA.

What is the generic name for Lamotrigine Extended-Release?

The generic name for Lamotrigine Extended-Release is lamotrigine. There are 11 other brand versions of lamotrigine.

What is the NDC code for Lamotrigine Extended-Release 300 mg/1?

The NDC (National Drug Code) for Lamotrigine Extended-Release 300 mg/1 is 10370-256, listed by Par Health USA, LLC.

Product NDC

10370-256

Package NDC

10370-256-11

Other Lamotrigine Extended-Release Dosages

Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.

Data from openFDA · Public domain (CC0 1.0)