# Lamotrigine

NDC: 0115-9940
Generic name: LAMOTRIGINE
Labeler / Manufacturer: Amneal Pharmaceuticals of New York LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, ORALLY DISINTEGRATING
Routes: ORAL
Marketing started: 20181227

FDA application: ANDA200828

## Active ingredients

- LAMOTRIGINE: 50 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0115-9940"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0115-9940
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9e5c2d76-47a6-4a57-b23c-2398b307380c