# Lamotrigine

NDC: 43598-552
Generic name: Lamotrigine
Labeler / Manufacturer: Dr. Reddys Laboratories Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, ORALLY DISINTEGRATING
Routes: ORAL
Marketing started: 20160617

FDA application: ANDA206382

## Active ingredients

- LAMOTRIGINE: 100 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"43598-552"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=43598-552
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=54ea1ec3-876b-4d3a-a92b-1a6d70951de0