# Lamotrigine

NDC: 70518-4702
Generic name: Lamotrigine
Labeler / Manufacturer: REMEDYREPACK INC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20260719

FDA application: ANDA207763

## Active ingredients

- LAMOTRIGINE: 50 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70518-4702"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70518-4702
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=fa679e97-3b3d-4bf2-8de7-da3a89e38b37