# LAMICTAL XR

NDC: 0173-0761
Generic name: lamotrigine
Labeler / Manufacturer: GlaxoSmithKline LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: TABLET, FILM COATED, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20110331

FDA application: NDA022115

## Active ingredients

- LAMOTRIGINE: 300 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0173-0761"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0173-0761
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=3e2c9a35-6a39-41d7-ad84-3c0bb8894b09