# Lamotrigine

NDC: 82804-105
Generic name: Lamotrigine
Labeler / Manufacturer: Proficient Rx LP
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20131223

FDA application: ANDA203370

## 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:"82804-105"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=82804-105
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ffa46cb2-16e7-45f3-9940-5cb88d0cda9d