# Lamotrigine

NDC: 71335-2071
Generic name: Lamotrigine
Labeler / Manufacturer: Bryant Ranch Prepack
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20090127

FDA application: ANDA078525

## Active ingredients

- LAMOTRIGINE: 150 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71335-2071"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71335-2071
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=68a4dac2-5015-40c5-88ca-204098c3b288