# Lamotrigine

NDC: 16571-786
Generic name: Lamotrigine
Labeler / Manufacturer: Rising Pharma Holdings, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, CHEWABLE
Routes: ORAL
Marketing started: 20091104

FDA application: ANDA090401

## 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:"16571-786"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=16571-786
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f54690b3-bcbb-4d94-95b9-b7591af00117