# Lamotrigine

NDC: 0228-1638
Generic name: Lamotrigine
Labeler / Manufacturer: Actavis Pharma, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20160601

FDA application: ANDA200672

## Active ingredients

- LAMOTRIGINE: 250 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0228-1638"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0228-1638
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=87beaf22-593d-4170-bb58-332c615ef90d