# Lamotrigine

NDC: 65162-988
Generic name: Lamotrigine
Labeler / Manufacturer: Amneal Pharmaceuticals LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20181130

FDA application: ANDA207497

## Active ingredients

- LAMOTRIGINE: 250 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"65162-988"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=65162-988
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=0833d3df-2df1-4abd-abe0-7fb2c0253c80