RecallHawk

MOTPOLY XR (LACOSAMIDE)

AUCTA

Summary

FDA approved MOTPOLY XR (LACOSAMIDE) by AUCTA. NDA (New Drug) approval (Efficacy) on 2024-06-07. CAPSULE, EXTENDED RELEASE, ORAL.

Details

Source

Drug Approval

External ID

NDA216185-1

Action Date

2024-06-07

Status

Approved

Category

drug

Product Code

NDA (New Drug)

Product Description

MOTPOLY XR (generic: LACOSAMIDE), CAPSULE, EXTENDED RELEASE, ORAL. Application: NDA216185

Company

Context & Analysis

AUCTA has 4 FDA actions in our database.

Frequently Asked Questions

How often does AUCTA have FDA actions?

AUCTA has 4 FDA actions in our database, including 0 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "NDA216185-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

Want to know the moment something like this happens?

Get alerts for drug

Related Actions