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# Impax Recalls 1 Lot of Lamotrigine Due to Packaging Error
- URL: https://www.fdaweb.com/impax-recalls-1-lot-of-lamotrigine-due-to-packaging-error/
- Published: 2016-08-29T12:00:00.000Z
- Updated: 2026-09-14T21:27:27.000Z
- Author: David McFarland
- Tags: Drugs, #legacy-id-D5136635

Impax Laboratories has recalled one lot of lamotrigine orally disintegrating tablets (ODT) 200 mg (Lot # 502240) due to a packaging error. The unit-of-use blister packs (a 10-count blister card contained in a single plastic shell-pack) may contain 100 mg product instead of the 200 mg product, according to a [recall notice](http://links.govdelivery.com/track?type=click&enid=ZWFzPTEmbWFpbGluZ2lkPTIwMTYwODI5LjYzMDk4MjYxJm1lc3NhZ2VpZD1NREItUFJELUJVTC0yMDE2MDgyOS42MzA5ODI2MSZkYXRhYmFzZWlkPTEwMDEmc2VyaWFsPTE3MzQwOTQzJmVtYWlsaWQ9ZGF2aWRAZmRhd2ViLmNvbSZ1c2VyaWQ9ZGF2aWRAZmRhd2ViLmNvbSZmbD0mZXh0cmE9TXVsdGl2YXJpYXRlSWQ9JiYm&&&103&&&http://www.fda.gov/Safety/MedWatch/SafetyInformation/SafetyAlertsforHumanMedicalProducts/ucm518486.htm?source=govdelivery&utm%5Fmedium=email&utm%5Fsource=govdelivery). “Each blister card within the unit-of-use blister pack is properly labeled as 100 mg ODT, however the plastic shell pack containing the 100 mg blister cards is labeled as 200 mg ODT,” it says. As a result, it is possible that consumers could take less than their intended lamotrigine dose. Lamotrigine is indicated for treating epilepsy and bipolar disorders.