# lamotrigine

NDC: 31722-243
Generic name: lamotrigine extended-release
Labeler / Manufacturer: Camber Pharmaceuticals Inc
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20211209

FDA application: ANDA213949

## Active ingredients

- LAMOTRIGINE: 200 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"31722-243"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=31722-243
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e45bd69f-3580-ff15-e053-2a95a90a4615