# Lamotrigine

NDC: 16714-623
Generic name: Lamotrigine
Labeler / Manufacturer: NorthStar Rx LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20170620

FDA application: ANDA202383

## Active ingredients

- LAMOTRIGINE: 25 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"16714-623"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=16714-623
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9ab07d6b-ae4a-a310-5572-b266676cd29e